LeishMANIAdb
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CHAP domain/Glutathionylspermidine synthase preATP-grasp, putative

Quick info Localization Expansion Sequence features Structure Function Putative motif mimicry Homologs Download

Quick info

Protein:
CHAP domain/Glutathionylspermidine synthase preATP-grasp, putative
Gene product:
glutathionylspermidine synthase, putative
Species:
Leishmania donovani
UniProt:
A0A3Q8IGS6_LEIDO
TriTrypDb:
LdBPK_252500.1 * , LdCL_250030900 , LDHU3_25.3000
Length:
719

Localization

Secreted promastigote
Source Evidence on protein Close homologs
Cuervo et al. no yes: 0
Hassani et al. no yes: 0
Forrest at al. (metacyclic) no yes: 0
Forrest at al. (procyclic) no yes: 0
Silverman et al. no yes: 0
Pissara et al. no yes: 0
Secreted amastigote
Source Evidence on protein Close homologs
Pires et al. no yes: 0
Exosome
Source Evidence on protein Close homologs
Silverman et al. no yes: 0
Glycosome
Source Evidence on protein Close homologs
Jamdhade et al. no yes: 0
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 4
NetGPI no yes: 0, no: 4
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

A0A3Q8IGS6
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A0A3Q8IGS6

Function

Could not find GO biological_process term for this entry.
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 2
GO:0008885 glutathionylspermidine synthase activity 5 2
GO:0016874 ligase activity 2 2
GO:0016879 ligase activity, forming carbon-nitrogen bonds 3 2
GO:0016880 acid-ammonia (or amide) ligase activity 4 2

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 216 220 PF00656 0.408
CLV_C14_Caspase3-7 315 319 PF00656 0.459
CLV_C14_Caspase3-7 511 515 PF00656 0.372
CLV_C14_Caspase3-7 691 695 PF00656 0.572
CLV_NRD_NRD_1 338 340 PF00675 0.372
CLV_NRD_NRD_1 61 63 PF00675 0.591
CLV_NRD_NRD_1 84 86 PF00675 0.562
CLV_NRD_NRD_1 89 91 PF00675 0.565
CLV_PCSK_KEX2_1 260 262 PF00082 0.525
CLV_PCSK_KEX2_1 338 340 PF00082 0.372
CLV_PCSK_KEX2_1 654 656 PF00082 0.445
CLV_PCSK_KEX2_1 84 86 PF00082 0.508
CLV_PCSK_PC1ET2_1 260 262 PF00082 0.525
CLV_PCSK_PC1ET2_1 654 656 PF00082 0.500
CLV_PCSK_SKI1_1 227 231 PF00082 0.492
CLV_PCSK_SKI1_1 538 542 PF00082 0.372
CLV_PCSK_SKI1_1 544 548 PF00082 0.372
CLV_PCSK_SKI1_1 654 658 PF00082 0.382
DEG_Nend_Nbox_1 1 3 PF02207 0.645
DOC_ANK_TNKS_1 260 267 PF00023 0.537
DOC_MAPK_gen_1 450 457 PF00069 0.348
DOC_MAPK_gen_1 62 68 PF00069 0.642
DOC_MAPK_gen_1 689 698 PF00069 0.463
DOC_MAPK_gen_1 701 709 PF00069 0.456
DOC_MAPK_MEF2A_6 106 114 PF00069 0.291
DOC_MAPK_MEF2A_6 450 457 PF00069 0.348
DOC_PP1_RVXF_1 419 426 PF00149 0.459
DOC_PP1_RVXF_1 454 461 PF00149 0.372
DOC_PP2B_LxvP_1 2 5 PF13499 0.641
DOC_PP4_FxxP_1 327 330 PF00568 0.372
DOC_PP4_MxPP_1 343 346 PF00568 0.372
DOC_USP7_MATH_1 126 130 PF00917 0.290
DOC_USP7_MATH_1 134 138 PF00917 0.258
DOC_USP7_MATH_1 298 302 PF00917 0.372
DOC_USP7_MATH_1 512 516 PF00917 0.459
DOC_USP7_MATH_1 56 60 PF00917 0.572
DOC_USP7_MATH_1 622 626 PF00917 0.631
DOC_USP7_MATH_1 628 632 PF00917 0.652
DOC_USP7_MATH_2 605 611 PF00917 0.521
DOC_USP7_UBL2_3 415 419 PF12436 0.459
DOC_USP7_UBL2_3 452 456 PF12436 0.372
DOC_USP7_UBL2_3 660 664 PF12436 0.448
DOC_USP7_UBL2_3 72 76 PF12436 0.339
DOC_WW_Pin1_4 106 111 PF00397 0.370
DOC_WW_Pin1_4 115 120 PF00397 0.297
DOC_WW_Pin1_4 145 150 PF00397 0.308
DOC_WW_Pin1_4 26 31 PF00397 0.436
DOC_WW_Pin1_4 48 53 PF00397 0.599
DOC_WW_Pin1_4 515 520 PF00397 0.348
LIG_14-3-3_CanoR_1 190 198 PF00244 0.567
LIG_14-3-3_CanoR_1 297 303 PF00244 0.372
LIG_14-3-3_CanoR_1 304 314 PF00244 0.372
LIG_14-3-3_CanoR_1 338 342 PF00244 0.372
LIG_14-3-3_CanoR_1 434 441 PF00244 0.372
LIG_14-3-3_CanoR_1 508 516 PF00244 0.380
LIG_BRCT_BRCA1_1 347 351 PF00533 0.381
LIG_BRCT_BRCA1_1 613 617 PF00533 0.655
LIG_Clathr_ClatBox_1 19 23 PF01394 0.563
LIG_DCNL_PONY_1 1 4 PF03556 0.647
LIG_deltaCOP1_diTrp_1 103 111 PF00928 0.311
LIG_FHA_1 107 113 PF00498 0.370
LIG_FHA_1 15 21 PF00498 0.508
LIG_FHA_1 155 161 PF00498 0.370
LIG_FHA_1 193 199 PF00498 0.472
LIG_FHA_1 308 314 PF00498 0.372
LIG_FHA_1 511 517 PF00498 0.380
LIG_FHA_1 566 572 PF00498 0.372
LIG_FHA_1 685 691 PF00498 0.450
LIG_FHA_2 116 122 PF00498 0.370
LIG_FHA_2 43 49 PF00498 0.485
LIG_FHA_2 518 524 PF00498 0.372
LIG_FHA_2 642 648 PF00498 0.556
LIG_FHA_2 689 695 PF00498 0.498
LIG_HCF-1_HBM_1 7 10 PF13415 0.660
LIG_Integrin_isoDGR_2 582 584 PF01839 0.372
LIG_LIR_Apic_2 245 251 PF02991 0.523
LIG_LIR_Apic_2 324 330 PF02991 0.372
LIG_LIR_Gen_1 108 119 PF02991 0.370
LIG_LIR_Gen_1 121 126 PF02991 0.291
LIG_LIR_Gen_1 340 347 PF02991 0.459
LIG_LIR_Gen_1 405 411 PF02991 0.372
LIG_LIR_Gen_1 41 52 PF02991 0.495
LIG_LIR_Gen_1 432 443 PF02991 0.459
LIG_LIR_Gen_1 496 506 PF02991 0.372
LIG_LIR_Nem_3 108 114 PF02991 0.370
LIG_LIR_Nem_3 121 125 PF02991 0.291
LIG_LIR_Nem_3 147 153 PF02991 0.308
LIG_LIR_Nem_3 224 229 PF02991 0.451
LIG_LIR_Nem_3 282 287 PF02991 0.426
LIG_LIR_Nem_3 324 329 PF02991 0.372
LIG_LIR_Nem_3 405 410 PF02991 0.372
LIG_LIR_Nem_3 41 47 PF02991 0.494
LIG_LIR_Nem_3 496 502 PF02991 0.372
LIG_LIR_Nem_3 51 57 PF02991 0.564
LIG_LIR_Nem_3 534 540 PF02991 0.372
LIG_LIR_Nem_3 662 668 PF02991 0.403
LIG_LIR_Nem_3 67 73 PF02991 0.336
LIG_LIR_Nem_3 675 681 PF02991 0.320
LIG_MYND_1 247 251 PF01753 0.524
LIG_PCNA_PIPBox_1 380 389 PF02747 0.348
LIG_Pex14_2 657 661 PF04695 0.381
LIG_REV1ctd_RIR_1 654 664 PF16727 0.522
LIG_SH2_CRK 54 58 PF00017 0.659
LIG_SH2_CRK 70 74 PF00017 0.210
LIG_SH2_STAP1 182 186 PF00017 0.522
LIG_SH2_STAT3 506 509 PF00017 0.372
LIG_SH2_STAT5 258 261 PF00017 0.506
LIG_SH2_STAT5 285 288 PF00017 0.391
LIG_SH2_STAT5 321 324 PF00017 0.394
LIG_SH2_STAT5 326 329 PF00017 0.348
LIG_SH2_STAT5 435 438 PF00017 0.372
LIG_SH2_STAT5 576 579 PF00017 0.372
LIG_SH2_STAT5 665 668 PF00017 0.397
LIG_SH2_STAT5 713 716 PF00017 0.584
LIG_SH2_STAT5 86 89 PF00017 0.308
LIG_SH3_3 226 232 PF00018 0.483
LIG_SH3_3 233 239 PF00018 0.377
LIG_SH3_3 241 247 PF00018 0.315
LIG_SH3_3 513 519 PF00018 0.353
LIG_SH3_3 529 535 PF00018 0.421
LIG_SH3_3 574 580 PF00018 0.473
LIG_SUMO_SIM_anti_2 195 202 PF11976 0.460
LIG_SUMO_SIM_anti_2 488 494 PF11976 0.381
LIG_SUMO_SIM_par_1 194 202 PF11976 0.466
LIG_SUMO_SIM_par_1 471 476 PF11976 0.432
LIG_SUMO_SIM_par_1 478 486 PF11976 0.377
LIG_SUMO_SIM_par_1 64 69 PF11976 0.396
LIG_TRAF2_1 604 607 PF00917 0.509
LIG_TRFH_1 327 331 PF08558 0.381
LIG_TYR_ITIM 68 73 PF00017 0.575
LIG_UBA3_1 616 620 PF00899 0.469
LIG_WRC_WIRS_1 57 62 PF05994 0.579
MOD_CDK_SPxxK_3 106 113 PF00069 0.314
MOD_CK1_1 145 151 PF00069 0.270
MOD_CK1_1 192 198 PF00069 0.563
MOD_CK1_1 394 400 PF00069 0.389
MOD_CK1_1 498 504 PF00069 0.372
MOD_CK1_1 515 521 PF00069 0.372
MOD_CK1_1 610 616 PF00069 0.657
MOD_CK1_1 641 647 PF00069 0.639
MOD_CK1_1 688 694 PF00069 0.436
MOD_CK2_1 115 121 PF00069 0.308
MOD_CK2_1 42 48 PF00069 0.468
MOD_CMANNOS 494 497 PF00535 0.372
MOD_DYRK1A_RPxSP_1 106 110 PF00069 0.314
MOD_GlcNHglycan 191 194 PF01048 0.602
MOD_GlcNHglycan 281 284 PF01048 0.484
MOD_GlcNHglycan 318 321 PF01048 0.372
MOD_GlcNHglycan 347 350 PF01048 0.381
MOD_GlcNHglycan 368 372 PF01048 0.312
MOD_GlcNHglycan 510 513 PF01048 0.459
MOD_GlcNHglycan 626 629 PF01048 0.702
MOD_GlcNHglycan 647 650 PF01048 0.549
MOD_GSK3_1 188 195 PF00069 0.579
MOD_GSK3_1 387 394 PF00069 0.340
MOD_GSK3_1 42 49 PF00069 0.485
MOD_GSK3_1 508 515 PF00069 0.404
MOD_GSK3_1 607 614 PF00069 0.547
MOD_GSK3_1 624 631 PF00069 0.486
MOD_GSK3_1 634 641 PF00069 0.454
MOD_GSK3_1 684 691 PF00069 0.416
MOD_N-GLC_1 126 131 PF02516 0.508
MOD_N-GLC_1 705 710 PF02516 0.585
MOD_N-GLC_2 529 531 PF02516 0.459
MOD_N-GLC_2 638 640 PF02516 0.543
MOD_NEK2_1 259 264 PF00069 0.428
MOD_NEK2_1 307 312 PF00069 0.459
MOD_NEK2_1 42 47 PF00069 0.581
MOD_NEK2_1 609 614 PF00069 0.642
MOD_NEK2_1 645 650 PF00069 0.509
MOD_NEK2_2 206 211 PF00069 0.492
MOD_NEK2_2 298 303 PF00069 0.372
MOD_PIKK_1 376 382 PF00454 0.372
MOD_PIKK_1 387 393 PF00454 0.372
MOD_PIKK_1 611 617 PF00454 0.570
MOD_PIKK_1 628 634 PF00454 0.619
MOD_PK_1 692 698 PF00069 0.553
MOD_PKA_2 14 20 PF00069 0.505
MOD_PKA_2 189 195 PF00069 0.589
MOD_PKA_2 337 343 PF00069 0.372
MOD_PKA_2 433 439 PF00069 0.372
MOD_Plk_1 120 126 PF00069 0.352
MOD_Plk_1 705 711 PF00069 0.594
MOD_Plk_4 394 400 PF00069 0.372
MOD_Plk_4 498 504 PF00069 0.372
MOD_Plk_4 641 647 PF00069 0.569
MOD_Plk_4 692 698 PF00069 0.466
MOD_ProDKin_1 106 112 PF00069 0.370
MOD_ProDKin_1 115 121 PF00069 0.297
MOD_ProDKin_1 145 151 PF00069 0.308
MOD_ProDKin_1 26 32 PF00069 0.439
MOD_ProDKin_1 48 54 PF00069 0.607
MOD_ProDKin_1 515 521 PF00069 0.348
MOD_SUMO_rev_2 59 65 PF00179 0.583
TRG_DiLeu_LyEn_5 332 337 PF01217 0.372
TRG_ENDOCYTIC_2 214 217 PF00928 0.527
TRG_ENDOCYTIC_2 326 329 PF00928 0.372
TRG_ENDOCYTIC_2 386 389 PF00928 0.459
TRG_ENDOCYTIC_2 435 438 PF00928 0.459
TRG_ENDOCYTIC_2 54 57 PF00928 0.667
TRG_ENDOCYTIC_2 665 668 PF00928 0.375
TRG_ENDOCYTIC_2 70 73 PF00928 0.337
TRG_ER_diArg_1 337 339 PF00400 0.372
TRG_ER_diArg_1 84 86 PF00400 0.311

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P5Y6 Leptomonas seymouri 27% 100%
A0A0N1PC88 Leptomonas seymouri 71% 100%
A0A0S4J0Y2 Bodo saltans 38% 82%
A0A0S4JSQ6 Bodo saltans 29% 100%
A0A1X0ND08 Trypanosomatidae 52% 100%
A0A1X0NR71 Trypanosomatidae 30% 100%
A0A3Q8IGF4 Leishmania donovani 28% 92%
A0A3R7LYC7 Trypanosoma rangeli 30% 100%
A4HFW1 Leishmania braziliensis 26% 91%
A4I1T8 Leishmania infantum 99% 100%
A4I2Z3 Leishmania infantum 29% 92%
C9ZJE1 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 31% 100%
E9AXX3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 93% 100%
E9AZ89 Leishmania mexicana (strain MHOM/GT/2001/U1103) 28% 92%
O60993 Crithidia fasciculata 28% 100%
P0AES0 Escherichia coli (strain K12) 27% 100%
P0AES1 Shigella flexneri 27% 100%
P90518 Crithidia fasciculata 70% 100%
Q711P7 Leishmania major 28% 92%
Q9GT49 Trypanosoma cruzi (strain CL Brener) 30% 100%
V5ASH7 Trypanosoma cruzi 49% 100%
V5AYP7 Trypanosoma cruzi 31% 100%

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LeishMANIAdb - Server version: v0.0.2. - Database version: v0.0.1. - ChangeLog - © 2022-2025 Protein Bioinformatics Research Group, Institute of Enzymology, RCNS