Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

6VCU

Homo sapiens FKBP12 protein bound with APX879 in P32 space group

Functional Information from GO Data
ChainGOidnamespacecontents
A0000413biological_processprotein peptidyl-prolyl isomerization
A0003007biological_processheart morphogenesis
A0003755molecular_functionpeptidyl-prolyl cis-trans isomerase activity
A0005160molecular_functiontransforming growth factor beta receptor binding
A0005515molecular_functionprotein binding
A0005527molecular_functionmacrolide binding
A0005528molecular_functionFK506 binding
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006457biological_processprotein folding
A0006458biological_process'de novo' protein folding
A0014802cellular_componentterminal cisterna
A0014809biological_processregulation of skeletal muscle contraction by regulation of release of sequestered calcium ion
A0016020cellular_componentmembrane
A0016247molecular_functionchannel regulator activity
A0016529cellular_componentsarcoplasmic reticulum
A0022417biological_processprotein maturation by protein folding
A0030018cellular_componentZ disc
A0030512biological_processnegative regulation of transforming growth factor beta receptor signaling pathway
A0030547molecular_functionsignaling receptor inhibitor activity
A0032092biological_processpositive regulation of protein binding
A0032880biological_processregulation of protein localization
A0032926biological_processnegative regulation of activin receptor signaling pathway
A0033017cellular_componentsarcoplasmic reticulum membrane
A0034713molecular_functiontype I transforming growth factor beta receptor binding
A0042026biological_processprotein refolding
A0042110biological_processT cell activation
A0043123biological_processpositive regulation of canonical NF-kappaB signal transduction
A0044325molecular_functiontransmembrane transporter binding
A0050776biological_processregulation of immune response
A0055010biological_processventricular cardiac muscle tissue morphogenesis
A0060314biological_processregulation of ryanodine-sensitive calcium-release channel activity
A0060347biological_processheart trabecula formation
A0070411molecular_functionI-SMAD binding
A0070588biological_processcalcium ion transmembrane transport
A0070697molecular_functionactivin receptor binding
A0097435biological_processsupramolecular fiber organization
A0098562cellular_componentcytoplasmic side of membrane
A1902991biological_processregulation of amyloid precursor protein catabolic process
A1990000biological_processamyloid fibril formation
A1990425cellular_componentryanodine receptor complex
B0000413biological_processprotein peptidyl-prolyl isomerization
B0003007biological_processheart morphogenesis
B0003755molecular_functionpeptidyl-prolyl cis-trans isomerase activity
B0005160molecular_functiontransforming growth factor beta receptor binding
B0005515molecular_functionprotein binding
B0005527molecular_functionmacrolide binding
B0005528molecular_functionFK506 binding
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0006457biological_processprotein folding
B0006458biological_process'de novo' protein folding
B0014802cellular_componentterminal cisterna
B0014809biological_processregulation of skeletal muscle contraction by regulation of release of sequestered calcium ion
B0016020cellular_componentmembrane
B0016247molecular_functionchannel regulator activity
B0016529cellular_componentsarcoplasmic reticulum
B0022417biological_processprotein maturation by protein folding
B0030018cellular_componentZ disc
B0030512biological_processnegative regulation of transforming growth factor beta receptor signaling pathway
B0030547molecular_functionsignaling receptor inhibitor activity
B0032092biological_processpositive regulation of protein binding
B0032880biological_processregulation of protein localization
B0032926biological_processnegative regulation of activin receptor signaling pathway
B0033017cellular_componentsarcoplasmic reticulum membrane
B0034713molecular_functiontype I transforming growth factor beta receptor binding
B0042026biological_processprotein refolding
B0042110biological_processT cell activation
B0043123biological_processpositive regulation of canonical NF-kappaB signal transduction
B0044325molecular_functiontransmembrane transporter binding
B0050776biological_processregulation of immune response
B0055010biological_processventricular cardiac muscle tissue morphogenesis
B0060314biological_processregulation of ryanodine-sensitive calcium-release channel activity
B0060347biological_processheart trabecula formation
B0070411molecular_functionI-SMAD binding
B0070588biological_processcalcium ion transmembrane transport
B0070697molecular_functionactivin receptor binding
B0097435biological_processsupramolecular fiber organization
B0098562cellular_componentcytoplasmic side of membrane
B1902991biological_processregulation of amyloid precursor protein catabolic process
B1990000biological_processamyloid fibril formation
B1990425cellular_componentryanodine receptor complex
C0000413biological_processprotein peptidyl-prolyl isomerization
C0003007biological_processheart morphogenesis
C0003755molecular_functionpeptidyl-prolyl cis-trans isomerase activity
C0005160molecular_functiontransforming growth factor beta receptor binding
C0005515molecular_functionprotein binding
C0005527molecular_functionmacrolide binding
C0005528molecular_functionFK506 binding
C0005737cellular_componentcytoplasm
C0005829cellular_componentcytosol
C0006457biological_processprotein folding
C0006458biological_process'de novo' protein folding
C0014802cellular_componentterminal cisterna
C0014809biological_processregulation of skeletal muscle contraction by regulation of release of sequestered calcium ion
C0016020cellular_componentmembrane
C0016247molecular_functionchannel regulator activity
C0016529cellular_componentsarcoplasmic reticulum
C0022417biological_processprotein maturation by protein folding
C0030018cellular_componentZ disc
C0030512biological_processnegative regulation of transforming growth factor beta receptor signaling pathway
C0030547molecular_functionsignaling receptor inhibitor activity
C0032092biological_processpositive regulation of protein binding
C0032880biological_processregulation of protein localization
C0032926biological_processnegative regulation of activin receptor signaling pathway
C0033017cellular_componentsarcoplasmic reticulum membrane
C0034713molecular_functiontype I transforming growth factor beta receptor binding
C0042026biological_processprotein refolding
C0042110biological_processT cell activation
C0043123biological_processpositive regulation of canonical NF-kappaB signal transduction
C0044325molecular_functiontransmembrane transporter binding
C0050776biological_processregulation of immune response
C0055010biological_processventricular cardiac muscle tissue morphogenesis
C0060314biological_processregulation of ryanodine-sensitive calcium-release channel activity
C0060347biological_processheart trabecula formation
C0070411molecular_functionI-SMAD binding
C0070588biological_processcalcium ion transmembrane transport
C0070697molecular_functionactivin receptor binding
C0097435biological_processsupramolecular fiber organization
C0098562cellular_componentcytoplasmic side of membrane
C1902991biological_processregulation of amyloid precursor protein catabolic process
C1990000biological_processamyloid fibril formation
C1990425cellular_componentryanodine receptor complex
D0000413biological_processprotein peptidyl-prolyl isomerization
D0003007biological_processheart morphogenesis
D0003755molecular_functionpeptidyl-prolyl cis-trans isomerase activity
D0005160molecular_functiontransforming growth factor beta receptor binding
D0005515molecular_functionprotein binding
D0005527molecular_functionmacrolide binding
D0005528molecular_functionFK506 binding
D0005737cellular_componentcytoplasm
D0005829cellular_componentcytosol
D0006457biological_processprotein folding
D0006458biological_process'de novo' protein folding
D0014802cellular_componentterminal cisterna
D0014809biological_processregulation of skeletal muscle contraction by regulation of release of sequestered calcium ion
D0016020cellular_componentmembrane
D0016247molecular_functionchannel regulator activity
D0016529cellular_componentsarcoplasmic reticulum
D0022417biological_processprotein maturation by protein folding
D0030018cellular_componentZ disc
D0030512biological_processnegative regulation of transforming growth factor beta receptor signaling pathway
D0030547molecular_functionsignaling receptor inhibitor activity
D0032092biological_processpositive regulation of protein binding
D0032880biological_processregulation of protein localization
D0032926biological_processnegative regulation of activin receptor signaling pathway
D0033017cellular_componentsarcoplasmic reticulum membrane
D0034713molecular_functiontype I transforming growth factor beta receptor binding
D0042026biological_processprotein refolding
D0042110biological_processT cell activation
D0043123biological_processpositive regulation of canonical NF-kappaB signal transduction
D0044325molecular_functiontransmembrane transporter binding
D0050776biological_processregulation of immune response
D0055010biological_processventricular cardiac muscle tissue morphogenesis
D0060314biological_processregulation of ryanodine-sensitive calcium-release channel activity
D0060347biological_processheart trabecula formation
D0070411molecular_functionI-SMAD binding
D0070588biological_processcalcium ion transmembrane transport
D0070697molecular_functionactivin receptor binding
D0097435biological_processsupramolecular fiber organization
D0098562cellular_componentcytoplasmic side of membrane
D1902991biological_processregulation of amyloid precursor protein catabolic process
D1990000biological_processamyloid fibril formation
D1990425cellular_componentryanodine receptor complex
Functional Information from PDB Data
site_idAC1
Number of Residues5
Detailsbinding site for residue ACT A 201
ChainResidue
AVAL4
AGLU5
ATHR6
AHOH388
BPRO93

site_idAC2
Number of Residues4
Detailsbinding site for residue ACT A 202
ChainResidue
AGLY1
AVAL2
ATYR80
AHOH385

site_idAC3
Number of Residues23
Detailsbinding site for residue R27 A 203
ChainResidue
ATYR26
APHE36
AASP37
AARG42
APHE46
AGLU54
AVAL55
AILE56
ATRP59
AALA81
ATYR82
AILE91
APHE99
AHOH311
BR27203
CTYR82
CTHR85
CGLY86
CHIS87
DPRO88
DR27202
DHOH322
DHOH352

site_idAC4
Number of Residues5
Detailsbinding site for residue ACT B 201
ChainResidue
APRO93
BVAL4
BGLU5
BTHR6
BHOH372

site_idAC5
Number of Residues3
Detailsbinding site for residue ACT B 202
ChainResidue
BGLY1
BVAL2
BTYR80

site_idAC6
Number of Residues22
Detailsbinding site for residue R27 B 203
ChainResidue
AR27203
BTYR26
BPHE36
BASP37
BARG42
BPHE46
BGLU54
BVAL55
BILE56
BTRP59
BALA81
BTYR82
BILE91
BPHE99
BHOH314
BHOH325
CPRO88
CR27201
DTYR82
DTHR85
DGLY86
DHIS87

site_idAC7
Number of Residues22
Detailsbinding site for residue R27 C 201
ChainResidue
ATYR82
ATHR85
AGLY86
AHIS87
BHIS87
BPRO88
BR27203
BHOH325
CTYR26
CPHE36
CASP37
CARG42
CPHE46
CGLU54
CVAL55
CILE56
CTRP59
CALA81
CTYR82
CILE91
CPHE99
DR27202

site_idAC8
Number of Residues6
Detailsbinding site for residue ACT D 201
ChainResidue
DHIS25
DASN43
DPRO45
DHOH308
DHOH333
DHOH389

site_idAC9
Number of Residues22
Detailsbinding site for residue R27 D 202
ChainResidue
DPHE36
DASP37
DARG42
DPHE46
DGLU54
DVAL55
DILE56
DTRP59
DALA81
DTYR82
DPHE99
DHOH322
DHOH352
AHIS87
APRO88
AR27203
BTYR82
BTHR85
BGLY86
BHIS87
CR27201
DTYR26

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsMOD_RES: N6-succinyllysine; alternate => ECO:0000250|UniProtKB:P26883
ChainResidueDetails
BLYS52
CLYS52
DLYS52
ALYS52

Catalytic Information from CSA
site_idMCSA1
Number of Residues6
DetailsM-CSA 362
ChainResidueDetails
ATYR26electrostatic destabiliser, steric role
APHE36electrostatic destabiliser, polar/non-polar interaction, steric role
AASP37electrostatic stabiliser, steric role
AILE56electrostatic stabiliser, steric role
ATYR82electrostatic stabiliser, steric role
APHE99electrostatic destabiliser, polar/non-polar interaction, steric role

site_idMCSA2
Number of Residues6
DetailsM-CSA 362
ChainResidueDetails
BTYR26electrostatic destabiliser, steric role
BPHE36electrostatic destabiliser, polar/non-polar interaction, steric role
BASP37electrostatic stabiliser, steric role
BILE56electrostatic stabiliser, steric role
BTYR82electrostatic stabiliser, steric role
BPHE99electrostatic destabiliser, polar/non-polar interaction, steric role

site_idMCSA3
Number of Residues6
DetailsM-CSA 362
ChainResidueDetails
CTYR26electrostatic destabiliser, steric role
CPHE36electrostatic destabiliser, polar/non-polar interaction, steric role
CASP37electrostatic stabiliser, steric role
CILE56electrostatic stabiliser, steric role
CTYR82electrostatic stabiliser, steric role
CPHE99electrostatic destabiliser, polar/non-polar interaction, steric role

site_idMCSA4
Number of Residues6
DetailsM-CSA 362
ChainResidueDetails
DTYR26electrostatic destabiliser, steric role
DPHE36electrostatic destabiliser, polar/non-polar interaction, steric role
DASP37electrostatic stabiliser, steric role
DILE56electrostatic stabiliser, steric role
DTYR82electrostatic stabiliser, steric role
DPHE99electrostatic destabiliser, polar/non-polar interaction, steric role

221051

PDB entries from 2024-06-12

PDB statisticsPDBj update infoContact PDBjnumon