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

6OIA

(1S,3S)-3-amino-4-(perfluoropropan-2-ylidene)cyclopentane-1-carboxylic acid hydrochloride, a potent inhibitor of ornithine aminotransferase

Functional Information from GO Data
ChainGOidnamespacecontents
A0004587molecular_functionornithine aminotransferase activity
A0005515molecular_functionprotein binding
A0005654cellular_componentnucleoplasm
A0005737cellular_componentcytoplasm
A0005739cellular_componentmitochondrion
A0005759cellular_componentmitochondrial matrix
A0007601biological_processvisual perception
A0008483molecular_functiontransaminase activity
A0010121biological_processarginine catabolic process to proline via ornithine
A0019544biological_processarginine catabolic process to glutamate
A0030170molecular_functionpyridoxal phosphate binding
A0042802molecular_functionidentical protein binding
A0055129biological_processL-proline biosynthetic process
B0004587molecular_functionornithine aminotransferase activity
B0005515molecular_functionprotein binding
B0005654cellular_componentnucleoplasm
B0005737cellular_componentcytoplasm
B0005739cellular_componentmitochondrion
B0005759cellular_componentmitochondrial matrix
B0007601biological_processvisual perception
B0008483molecular_functiontransaminase activity
B0010121biological_processarginine catabolic process to proline via ornithine
B0019544biological_processarginine catabolic process to glutamate
B0030170molecular_functionpyridoxal phosphate binding
B0042802molecular_functionidentical protein binding
B0055129biological_processL-proline biosynthetic process
C0004587molecular_functionornithine aminotransferase activity
C0005515molecular_functionprotein binding
C0005654cellular_componentnucleoplasm
C0005737cellular_componentcytoplasm
C0005739cellular_componentmitochondrion
C0005759cellular_componentmitochondrial matrix
C0007601biological_processvisual perception
C0008483molecular_functiontransaminase activity
C0010121biological_processarginine catabolic process to proline via ornithine
C0019544biological_processarginine catabolic process to glutamate
C0030170molecular_functionpyridoxal phosphate binding
C0042802molecular_functionidentical protein binding
C0055129biological_processL-proline biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues13
Detailsbinding site for residue PLP A 501
ChainResidue
AGLY142
AHOH674
AHOH739
BTHR322
BHOH642
AVAL143
APHE177
ATRP178
AASP263
AILE265
AGLN266
ALYS292
AHOH627

site_idAC2
Number of Residues9
Detailsbinding site for residue GOL A 502
ChainResidue
ATYR166
ALYS167
APRO202
AHOH711
AHOH734
AHOH750
AHOH761
AHOH765
CGLN220

site_idAC3
Number of Residues16
Detailsbinding site for residue PLP B 501
ChainResidue
ATHR322
AHOH608
BTHR141
BGLY142
BVAL143
BPHE177
BTRP178
BASP263
BILE265
BGLN266
BLYS292
BMQ4503
BHOH687
BHOH752
BHOH799
BHOH845

site_idAC4
Number of Residues7
Detailsbinding site for residue GOL B 502
ChainResidue
BILE206
BILE207
BHOH608
BHOH883
CTHR189
CPRO208
CHOH764

site_idAC5
Number of Residues20
Detailsbinding site for Di-peptide MQ4 B 503 and LYS B 292
ChainResidue
ASER321
ATHR322
ATYR323
BTYR55
BTYR85
BPHE177
BGLU235
BILE265
BGLN266
BGLY291
BALA293
BLEU294
BSER295
BARG413
BPLP501
BHOH604
BHOH656
BHOH673
BHOH792
BHOH799

site_idAC6
Number of Residues21
Detailsbinding site for residues PLP C 501 and MQ4 C 502
ChainResidue
CTYR55
CTYR85
CTHR141
CGLY142
CVAL143
CPHE177
CTRP178
CGLU235
CASP263
CILE265
CGLN266
CLYS292
CSER321
CTHR322
CARG413
CHOH625
CHOH654
CHOH662
CHOH677
CHOH740
CHOH770

site_idAC7
Number of Residues20
Detailsbinding site for Di-peptide MQ4 C 502 and LYS C 292
ChainResidue
CTYR323
CARG413
CPLP501
CHOH662
CHOH711
CHOH740
CHOH770
CTYR55
CTYR85
CALA87
CPHE177
CGLU235
CILE265
CGLN266
CGLY291
CALA293
CLEU294
CSER295
CSER321
CTHR322

Functional Information from PROSITE/UniProt
site_idPS00600
Number of Residues38
DetailsAA_TRANSFER_CLASS_3 Aminotransferases class-III pyridoxal-phosphate attachment site. FIaDEIqt.GLaRtGrwlavdyenvrp....DIVllGKalsGG
ChainResidueDetails
APHE260-GLY297

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues15
DetailsMOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:P29758
ChainResidueDetails
ALYS49
ALYS66
ALYS386
ALYS392
ALYS421
BLYS49
BLYS66
BLYS386
BLYS392
BLYS421
CLYS49
CLYS66
CLYS386
CLYS392
CLYS421

site_idSWS_FT_FI2
Number of Residues3
DetailsMOD_RES: N6-succinyllysine => ECO:0000250|UniProtKB:P29758
ChainResidueDetails
ALYS102
BLYS102
CLYS102

site_idSWS_FT_FI3
Number of Residues9
DetailsMOD_RES: N6-succinyllysine; alternate => ECO:0000250|UniProtKB:P29758
ChainResidueDetails
ALYS107
ALYS362
ALYS405
BLYS107
BLYS362
BLYS405
CLYS107
CLYS362
CLYS405

site_idSWS_FT_FI4
Number of Residues3
DetailsMOD_RES: N6-(pyridoxal phosphate)lysine => ECO:0000269|PubMed:3754226
ChainResidueDetails
ALYS292
BLYS292
CLYS292

Catalytic Information from CSA
site_idMCSA1
Number of Residues3
DetailsM-CSA 929
ChainResidueDetails
APHE177steric role
AASP263electrostatic stabiliser
ALYS292covalent catalysis, proton shuttle (general acid/base)

site_idMCSA2
Number of Residues3
DetailsM-CSA 929
ChainResidueDetails
BPHE177steric role
BASP263electrostatic stabiliser
BLYS292covalent catalysis, proton shuttle (general acid/base)

site_idMCSA3
Number of Residues3
DetailsM-CSA 929
ChainResidueDetails
CPHE177steric role
CASP263electrostatic stabiliser
CLYS292covalent catalysis, proton shuttle (general acid/base)

221051

PDB entries from 2024-06-12

PDB statisticsPDBj update infoContact PDBjnumon