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6YVY

FOCAL ADHESION KINASE CATALYTIC DOMAIN IN COMPLEX WITH 4-{[4-{[(1R,2R)-2-(dimethylamino)cyclopentyl]amino}-5-(trifluoromethyl)pyrimidin-2-yl]amino}-N-methylbenzenesulfonamide

Functional Information from GO Data
ChainGOidnamespacecontents
A0004672molecular_functionprotein kinase activity
A0004713molecular_functionprotein tyrosine kinase activity
A0005524molecular_functionATP binding
A0006468biological_processprotein phosphorylation
B0004672molecular_functionprotein kinase activity
B0004713molecular_functionprotein tyrosine kinase activity
B0005524molecular_functionATP binding
B0006468biological_processprotein phosphorylation
C0004672molecular_functionprotein kinase activity
C0004713molecular_functionprotein tyrosine kinase activity
C0005524molecular_functionATP binding
C0006468biological_processprotein phosphorylation
D0004672molecular_functionprotein kinase activity
D0004713molecular_functionprotein tyrosine kinase activity
D0005524molecular_functionATP binding
D0006468biological_processprotein phosphorylation
Functional Information from PDB Data
site_idAC1
Number of Residues18
Detailsbinding site for residue P1E A 701
ChainResidue
AARG426
ACYS502
ATHR503
AGLY505
AGLU506
ALEU553
AASP662
AARG665
AHOH881
AHOH886
AILE428
AGLU430
AVAL436
AALA452
ALYS454
AMET499
AGLU500
ALEU501

site_idAC2
Number of Residues17
Detailsbinding site for residue P1E B 701
ChainResidue
BARG426
BILE428
BGLU430
BVAL436
BALA452
BLYS454
BVAL484
BMET499
BGLU500
BLEU501
BCYS502
BTHR503
BGLY505
BGLU506
BLEU553
BHOH806
CGLN624

site_idAC3
Number of Residues7
Detailsbinding site for residue SO4 C 801
ChainResidue
BSER601
BARG668
CSER601
CARG668
CHOH903
CHOH966
CHOH992

site_idAC4
Number of Residues15
Detailsbinding site for residue P1E C 802
ChainResidue
BTYR516
BSER517
CARG426
CILE428
CGLU430
CVAL436
CMET499
CGLU500
CLEU501
CCYS502
CTHR503
CGLY505
CLEU553
CASP564
CHOH910

site_idAC5
Number of Residues16
Detailsbinding site for residue P1E D 701
ChainResidue
DARG426
DILE428
DGLU430
DVAL436
DALA452
DMET499
DGLU500
DLEU501
DCYS502
DTHR503
DGLY505
DGLU506
DARG550
DLEU553
DASP564
DHOH809

Functional Information from PROSITE/UniProt
site_idPS00107
Number of Residues27
DetailsPROTEIN_KINASE_ATP Protein kinases ATP-binding region signature. IGEGQFGDVHqGiymspenpala.......VAIK
ChainResidueDetails
AILE428-LYS454

site_idPS00109
Number of Residues13
DetailsPROTEIN_KINASE_TYR Tyrosine protein kinases specific active-site signature. FVHrDIAARNVLV
ChainResidueDetails
APHE542-VAL554

site_idPS00661
Number of Residues31
DetailsFERM_2 FERM domain signature 2. HrdiaarnvlVSsndCVklgDfgLsrYMeDS
ChainResidueDetails
AHIS544-SER574

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton acceptor => ECO:0000255|PROSITE-ProRule:PRU00159, ECO:0000255|PROSITE-ProRule:PRU10028
ChainResidueDetails
AASP546
BASP546
CASP546
DASP546

site_idSWS_FT_FI2
Number of Residues12
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU00159, ECO:0000269|PubMed:12467573
ChainResidueDetails
BLYS454
BGLU500
CILE428
CLYS454
CGLU500
DILE428
DLYS454
DGLU500
ALYS454
AGLU500
BILE428
AILE428

site_idSWS_FT_FI3
Number of Residues4
DetailsMOD_RES: Phosphotyrosine => ECO:0007744|PubMed:19369195
ChainResidueDetails
BTYR570
CTYR570
DTYR570
ATYR570

site_idSWS_FT_FI4
Number of Residues4
DetailsMOD_RES: Phosphotyrosine; by RET and SRC => ECO:0000269|PubMed:15561106, ECO:0000269|PubMed:19339212, ECO:0000269|PubMed:21454698
ChainResidueDetails
BTYR576
CTYR576
DTYR576
ATYR576

site_idSWS_FT_FI5
Number of Residues4
DetailsMOD_RES: Phosphotyrosine; by RET and SRC => ECO:0000269|PubMed:12387730, ECO:0000269|PubMed:19339212, ECO:0000269|PubMed:21454698
ChainResidueDetails
CTYR577
DTYR577
ATYR577
BTYR577

site_idSWS_FT_FI6
Number of Residues4
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:19369195
ChainResidueDetails
BSER580
CSER580
DSER580
ASER580

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PDB entries from 2024-05-15

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