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5T8K

1.95 Angstrom Crystal Structure of S-adenosylhomocysteinase from Cryptosporidium parvum in Complex with Adenine and NAD

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0004013molecular_functionadenosylhomocysteinase activity
A0005829cellular_componentcytosol
A0006730biological_processone-carbon metabolic process
A0016787molecular_functionhydrolase activity
A0033353biological_processS-adenosylmethionine cycle
B0000166molecular_functionnucleotide binding
B0004013molecular_functionadenosylhomocysteinase activity
B0005829cellular_componentcytosol
B0006730biological_processone-carbon metabolic process
B0016787molecular_functionhydrolase activity
B0033353biological_processS-adenosylmethionine cycle
C0000166molecular_functionnucleotide binding
C0004013molecular_functionadenosylhomocysteinase activity
C0005829cellular_componentcytosol
C0006730biological_processone-carbon metabolic process
C0016787molecular_functionhydrolase activity
C0033353biological_processS-adenosylmethionine cycle
D0000166molecular_functionnucleotide binding
D0004013molecular_functionadenosylhomocysteinase activity
D0005829cellular_componentcytosol
D0006730biological_processone-carbon metabolic process
D0016787molecular_functionhydrolase activity
D0033353biological_processS-adenosylmethionine cycle
Functional Information from PDB Data
site_idAC1
Number of Residues6
Detailsbinding site for residue NA A 501
ChainResidue
AGLU57
ATHR408
AGLY409
AHIS410
AADE503
AHOH717

site_idAC2
Number of Residues32
Detailsbinding site for residue NAD A 502
ChainResidue
AASN246
AGLY275
AGLY277
AGLU278
AVAL279
ATHR297
AGLU298
AILE299
AASP300
ACYS303
ATHR331
AGLY332
AASN333
AVAL336
AILE354
AGLY355
AHIS356
AASN403
AHIS410
AADE503
AHOH625
AHOH731
AHOH744
AHOH824
AHOH827
AHOH872
AHOH928
CLYS489
CTYR493
ATHR212
ATHR213
ATHR214

site_idAC3
Number of Residues12
Detailsbinding site for residue ADE A 503
ChainResidue
ALEU52
AHIS53
ATHR55
AGLU57
ATHR58
ATHR408
AGLY409
AHIS410
AMET415
ANA501
ANAD502
AHOH622

site_idAC4
Number of Residues3
Detailsbinding site for residue P6G A 504
ChainResidue
ALYS36
AGLU452
ATYR456

site_idAC5
Number of Residues3
Detailsbinding site for residue TRS A 505
ChainResidue
AILE7
ALYS8
ATRP101

site_idAC6
Number of Residues4
Detailsbinding site for residue GOL A 506
ChainResidue
ATYR206
AARG433
AGLU434
AVAL436

site_idAC7
Number of Residues6
Detailsbinding site for residue NA B 501
ChainResidue
BGLU57
BTHR408
BGLY409
BHIS410
BADE503
BHOH880

site_idAC8
Number of Residues32
Detailsbinding site for residue NAD B 502
ChainResidue
BTHR212
BTHR213
BTHR214
BASN246
BGLY275
BGLY277
BGLU278
BVAL279
BTHR297
BGLU298
BILE299
BASP300
BCYS303
BTHR331
BGLY332
BASN333
BVAL336
BILE354
BGLY355
BHIS356
BASN403
BHIS410
BADE503
BHOH624
BHOH776
BHOH785
BHOH792
BHOH793
BHOH863
BHOH925
DLYS489
DTYR493

site_idAC9
Number of Residues12
Detailsbinding site for residue ADE B 503
ChainResidue
BHIS53
BTHR55
BGLU57
BTHR58
BTHR408
BGLY409
BHIS410
BMET415
BNA501
BNAD502
BHOH620
BLEU52

site_idAD1
Number of Residues6
Detailsbinding site for residue P6G B 504
ChainResidue
BASN481
BPRO487
BLYS489
BSER490
BHOH806
DSER224

site_idAD2
Number of Residues3
Detailsbinding site for residue PEG B 505
ChainResidue
BLYS36
BTYR37
BHOH889

site_idAD3
Number of Residues9
Detailsbinding site for residue GOL B 506
ChainResidue
BARG218
BPHE357
BASP359
BHOH643
BHOH718
BHOH736
BHOH740
BHOH854
DTYR479

site_idAD4
Number of Residues6
Detailsbinding site for residue NA C 501
ChainResidue
CGLU57
CTHR408
CGLY409
CHIS410
CADE503
CHOH859

site_idAD5
Number of Residues33
Detailsbinding site for residue NAD C 502
ChainResidue
ALYS489
ATYR493
CTHR212
CTHR213
CTHR214
CASN246
CGLY275
CGLY277
CGLU278
CVAL279
CTHR297
CGLU298
CILE299
CASP300
CCYS303
CTHR331
CGLY332
CASN333
CVAL336
CILE354
CGLY355
CHIS356
CLEU401
CASN403
CHIS410
CADE503
CHOH712
CHOH734
CHOH812
CHOH831
CHOH861
CHOH877
CHOH954

site_idAD6
Number of Residues12
Detailsbinding site for residue ADE C 503
ChainResidue
CLEU52
CHIS53
CTHR55
CGLU57
CTHR58
CTHR408
CGLY409
CHIS410
CMET415
CNA501
CNAD502
CHOH670

site_idAD7
Number of Residues7
Detailsbinding site for residue P6G C 504
ChainResidue
ASER224
CASN481
CVAL482
CSER483
CPRO487
CLYS489
CHOH878

site_idAD8
Number of Residues4
Detailsbinding site for residue P6G C 505
ChainResidue
CLYS36
CTYR37
CLEU453
CHOH880

site_idAD9
Number of Residues1
Detailsbinding site for residue PEG C 506
ChainResidue
CILE7

site_idAE1
Number of Residues4
Detailsbinding site for residue PEG C 507
ChainResidue
CTYR206
CARG433
CGLU434
CVAL436

site_idAE2
Number of Residues6
Detailsbinding site for residue NA D 501
ChainResidue
DGLU57
DTHR408
DGLY409
DHIS410
DADE503
DHOH950

site_idAE3
Number of Residues33
Detailsbinding site for residue NAD D 502
ChainResidue
BLYS489
BTYR493
DTHR212
DTHR213
DTHR214
DASN246
DGLY275
DGLY277
DGLU278
DVAL279
DTHR297
DGLU298
DILE299
DASP300
DCYS303
DTHR331
DGLY332
DASN333
DVAL336
DILE354
DGLY355
DHIS356
DASN403
DHIS410
DADE503
DHOH629
DHOH771
DHOH792
DHOH797
DHOH802
DHOH862
DHOH872
DHOH929

site_idAE4
Number of Residues12
Detailsbinding site for residue ADE D 503
ChainResidue
DLEU52
DHIS53
DTHR55
DGLU57
DTHR58
DTHR408
DGLY409
DHIS410
DMET415
DNA501
DNAD502
DHOH624

site_idAE5
Number of Residues3
Detailsbinding site for residue PGE D 504
ChainResidue
DLYS36
DTYR37
DTYR456

site_idAE6
Number of Residues2
Detailsbinding site for residue PGE D 505
ChainResidue
DASN481
DSER490

site_idAE7
Number of Residues3
Detailsbinding site for residue PEG D 506
ChainResidue
DILE7
DTRP101
DHOH736

Functional Information from PROSITE/UniProt
site_idPS00738
Number of Residues15
DetailsADOHCYASE_1 S-adenosyl-L-homocysteine hydrolase signature 1. SCNiYSTQDhAAAAL
ChainResidueDetails
ASER76-LEU90
CSER76-LEU90

site_idPS00739
Number of Residues17
DetailsADOHCYASE_2 S-adenosyl-L-homocysteine hydrolase signature 2. GKkivVlGYGeVGKGc.A
ChainResidueDetails
AGLY268-ALA284
CGLY268-ALA284

227344

PDB entries from 2024-11-13

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