LeishMANIAdb
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Soluble_NSF_attachment_protein_-_SNAP_-_putative

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

Quick info

Protein:
Soluble_NSF_attachment_protein_-_SNAP_-_putative
Gene product:
Soluble NSF attachment protein - SNAP - putative
Species:
Leishmania infantum
UniProt:
A4HRM8_LEIIN
TriTrypDb:
LINF_020008100
Length:
690

Annotations

Annotations by Jardim et al.

Intracellular protein trafficking, Soluble NSF attachment , SNAP

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) yes yes: 2
Forrest at al. (procyclic) yes yes: 2
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: 5
NetGPI no yes: 0, no: 5
Cellular components
Term Name Level Count
GO:0031201 SNARE complex 3 1
GO:0032991 protein-containing complex 1 1
GO:0098796 membrane protein complex 2 1

Expansion

Sequence features

A4HRM8
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HRM8

Function

Biological processes
Term Name Level Count
GO:0006810 transport 3 6
GO:0006886 intracellular protein transport 4 6
GO:0008104 protein localization 4 6
GO:0009987 cellular process 1 6
GO:0015031 protein transport 4 6
GO:0033036 macromolecule localization 2 6
GO:0045184 establishment of protein localization 3 6
GO:0046907 intracellular transport 3 6
GO:0051179 localization 1 6
GO:0051234 establishment of localization 2 6
GO:0051641 cellular localization 2 6
GO:0051649 establishment of localization in cell 3 6
GO:0070727 cellular macromolecule localization 3 6
GO:0071702 organic substance transport 4 6
GO:0071705 nitrogen compound transport 4 6
GO:0016043 cellular component organization 3 1
GO:0022411 cellular component disassembly 4 1
GO:0032984 protein-containing complex disassembly 5 1
GO:0035494 SNARE complex disassembly 6 1
GO:0043933 protein-containing complex organization 4 1
GO:0071840 cellular component organization or biogenesis 2 1
Molecular functions
Term Name Level Count
GO:0000149 SNARE binding 3 1
GO:0005483 soluble NSF attachment protein activity 3 1
GO:0005488 binding 1 1
GO:0005515 protein binding 2 1
GO:0019905 syntaxin binding 4 1
GO:0030674 protein-macromolecule adaptor activity 2 1
GO:0060090 molecular adaptor activity 1 1

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 219 223 PF00656 0.729
CLV_C14_Caspase3-7 28 32 PF00656 0.643
CLV_C14_Caspase3-7 304 308 PF00656 0.418
CLV_C14_Caspase3-7 516 520 PF00656 0.547
CLV_MEL_PAP_1 241 247 PF00089 0.667
CLV_NRD_NRD_1 189 191 PF00675 0.701
CLV_NRD_NRD_1 264 266 PF00675 0.418
CLV_NRD_NRD_1 411 413 PF00675 0.636
CLV_NRD_NRD_1 573 575 PF00675 0.582
CLV_NRD_NRD_1 679 681 PF00675 0.633
CLV_PCSK_KEX2_1 188 190 PF00082 0.695
CLV_PCSK_KEX2_1 264 266 PF00082 0.418
CLV_PCSK_KEX2_1 411 413 PF00082 0.628
CLV_PCSK_KEX2_1 679 681 PF00082 0.633
CLV_PCSK_KEX2_1 90 92 PF00082 0.737
CLV_PCSK_PC1ET2_1 90 92 PF00082 0.691
CLV_PCSK_SKI1_1 289 293 PF00082 0.470
CLV_PCSK_SKI1_1 310 314 PF00082 0.470
CLV_PCSK_SKI1_1 393 397 PF00082 0.470
CLV_PCSK_SKI1_1 557 561 PF00082 0.514
CLV_PCSK_SKI1_1 616 620 PF00082 0.542
CLV_PCSK_SKI1_1 638 642 PF00082 0.534
CLV_PCSK_SKI1_1 680 684 PF00082 0.630
DEG_APCC_DBOX_1 521 529 PF00400 0.505
DEG_APCC_KENBOX_2 631 635 PF00400 0.561
DOC_ANK_TNKS_1 272 279 PF00023 0.327
DOC_CYCLIN_RxL_1 307 316 PF00134 0.470
DOC_CYCLIN_RxL_1 551 563 PF00134 0.533
DOC_CYCLIN_RxL_1 677 687 PF00134 0.632
DOC_MAPK_gen_1 522 531 PF00069 0.510
DOC_MAPK_MEF2A_6 340 348 PF00069 0.470
DOC_MAPK_MEF2A_6 522 531 PF00069 0.510
DOC_MAPK_MEF2A_6 591 598 PF00069 0.574
DOC_PP1_RVXF_1 287 294 PF00149 0.470
DOC_PP2B_PxIxI_1 343 349 PF00149 0.470
DOC_PP4_FxxP_1 468 471 PF00568 0.681
DOC_USP7_MATH_1 111 115 PF00917 0.746
DOC_USP7_MATH_1 140 144 PF00917 0.589
DOC_USP7_MATH_1 165 169 PF00917 0.728
DOC_USP7_MATH_1 194 198 PF00917 0.728
DOC_USP7_MATH_1 217 221 PF00917 0.739
DOC_USP7_MATH_1 243 247 PF00917 0.682
DOC_USP7_MATH_1 25 29 PF00917 0.634
DOC_USP7_MATH_1 294 298 PF00917 0.418
DOC_USP7_MATH_1 347 351 PF00917 0.475
DOC_USP7_MATH_1 439 443 PF00917 0.814
DOC_USP7_MATH_1 77 81 PF00917 0.776
DOC_WW_Pin1_4 220 225 PF00397 0.825
DOC_WW_Pin1_4 232 237 PF00397 0.685
DOC_WW_Pin1_4 247 252 PF00397 0.719
DOC_WW_Pin1_4 429 434 PF00397 0.721
DOC_WW_Pin1_4 447 452 PF00397 0.566
DOC_WW_Pin1_4 467 472 PF00397 0.678
DOC_WW_Pin1_4 590 595 PF00397 0.669
LIG_14-3-3_CanoR_1 244 251 PF00244 0.685
LIG_14-3-3_CanoR_1 264 274 PF00244 0.467
LIG_14-3-3_CanoR_1 508 514 PF00244 0.599
LIG_14-3-3_CanoR_1 569 574 PF00244 0.575
LIG_14-3-3_CanoR_1 645 650 PF00244 0.613
LIG_14-3-3_CanoR_1 679 683 PF00244 0.503
LIG_Actin_WH2_2 325 342 PF00022 0.470
LIG_APCC_ABBA_1 396 401 PF00400 0.470
LIG_BIR_II_1 1 5 PF00653 0.735
LIG_BIR_III_4 226 230 PF00653 0.699
LIG_BRCT_BRCA1_1 177 181 PF00533 0.632
LIG_BRCT_BRCA1_1 191 195 PF00533 0.682
LIG_BRCT_BRCA1_1 495 499 PF00533 0.778
LIG_BRCT_BRCA1_1 79 83 PF00533 0.710
LIG_deltaCOP1_diTrp_1 283 292 PF00928 0.470
LIG_FHA_1 144 150 PF00498 0.719
LIG_FHA_1 199 205 PF00498 0.716
LIG_FHA_1 286 292 PF00498 0.470
LIG_FHA_1 420 426 PF00498 0.611
LIG_FHA_1 430 436 PF00498 0.612
LIG_FHA_1 472 478 PF00498 0.709
LIG_FHA_1 484 490 PF00498 0.685
LIG_FHA_1 554 560 PF00498 0.522
LIG_FHA_1 561 567 PF00498 0.456
LIG_FHA_1 591 597 PF00498 0.580
LIG_FHA_2 125 131 PF00498 0.643
LIG_FHA_2 198 204 PF00498 0.685
LIG_FHA_2 266 272 PF00498 0.444
LIG_FHA_2 442 448 PF00498 0.753
LIG_FHA_2 648 654 PF00498 0.481
LIG_LIR_Apic_2 465 471 PF02991 0.679
LIG_LIR_Gen_1 235 245 PF02991 0.658
LIG_LIR_Gen_1 297 306 PF02991 0.418
LIG_LIR_Gen_1 605 612 PF02991 0.521
LIG_LIR_Gen_1 615 625 PF02991 0.479
LIG_LIR_Gen_1 681 690 PF02991 0.535
LIG_LIR_Gen_1 89 100 PF02991 0.669
LIG_LIR_Nem_3 192 198 PF02991 0.730
LIG_LIR_Nem_3 235 241 PF02991 0.654
LIG_LIR_Nem_3 297 302 PF02991 0.418
LIG_LIR_Nem_3 520 526 PF02991 0.439
LIG_LIR_Nem_3 556 561 PF02991 0.536
LIG_LIR_Nem_3 605 611 PF02991 0.518
LIG_LIR_Nem_3 615 621 PF02991 0.464
LIG_LIR_Nem_3 89 95 PF02991 0.672
LIG_LYPXL_SIV_4 266 274 PF13949 0.444
LIG_MYND_1 433 437 PF01753 0.677
LIG_NRBOX 524 530 PF00104 0.501
LIG_PCNA_yPIPBox_3 23 34 PF02747 0.652
LIG_PCNA_yPIPBox_3 630 641 PF02747 0.497
LIG_PTAP_UEV_1 450 455 PF05743 0.722
LIG_PTB_Apo_2 316 323 PF02174 0.470
LIG_SH2_CRK 159 163 PF00017 0.589
LIG_SH2_CRK 238 242 PF00017 0.656
LIG_SH2_CRK 561 565 PF00017 0.492
LIG_SH2_NCK_1 238 242 PF00017 0.656
LIG_SH2_NCK_1 267 271 PF00017 0.444
LIG_SH2_SRC 535 538 PF00017 0.537
LIG_SH2_STAT3 358 361 PF00017 0.418
LIG_SH2_STAT5 267 270 PF00017 0.498
LIG_SH2_STAT5 558 561 PF00017 0.545
LIG_SH2_STAT5 607 610 PF00017 0.536
LIG_SH3_1 591 597 PF00018 0.580
LIG_SH3_3 11 17 PF00018 0.756
LIG_SH3_3 230 236 PF00018 0.683
LIG_SH3_3 430 436 PF00018 0.672
LIG_SH3_3 448 454 PF00018 0.585
LIG_SH3_3 461 467 PF00018 0.572
LIG_SH3_3 494 500 PF00018 0.709
LIG_SH3_3 575 581 PF00018 0.629
LIG_SH3_3 591 597 PF00018 0.515
LIG_SUMO_SIM_par_1 230 235 PF11976 0.625
LIG_SUMO_SIM_par_1 524 530 PF11976 0.470
LIG_TRAF2_1 269 272 PF00917 0.418
LIG_TRAF2_1 384 387 PF00917 0.418
LIG_TYR_ITIM 559 564 PF00017 0.495
LIG_UBA3_1 377 385 PF00899 0.418
LIG_WW_1 504 507 PF00397 0.703
LIG_WW_2 433 436 PF00397 0.672
MOD_CDK_SPK_2 467 472 PF00069 0.678
MOD_CK1_1 118 124 PF00069 0.692
MOD_CK1_1 143 149 PF00069 0.556
MOD_CK1_1 197 203 PF00069 0.738
MOD_CK1_1 220 226 PF00069 0.737
MOD_CK1_1 470 476 PF00069 0.709
MOD_CK1_1 484 490 PF00069 0.645
MOD_CK1_1 76 82 PF00069 0.769
MOD_CK2_1 124 130 PF00069 0.641
MOD_CK2_1 197 203 PF00069 0.716
MOD_CK2_1 213 219 PF00069 0.717
MOD_CK2_1 265 271 PF00069 0.444
MOD_CK2_1 452 458 PF00069 0.627
MOD_CK2_1 660 666 PF00069 0.555
MOD_CK2_1 678 684 PF00069 0.499
MOD_GlcNHglycan 117 120 PF01048 0.724
MOD_GlcNHglycan 164 168 PF01048 0.783
MOD_GlcNHglycan 191 194 PF01048 0.689
MOD_GlcNHglycan 215 218 PF01048 0.748
MOD_GlcNHglycan 219 222 PF01048 0.723
MOD_GlcNHglycan 226 230 PF01048 0.671
MOD_GlcNHglycan 3 6 PF01048 0.760
MOD_GlcNHglycan 42 45 PF01048 0.778
MOD_GlcNHglycan 437 440 PF01048 0.748
MOD_GlcNHglycan 454 457 PF01048 0.581
MOD_GlcNHglycan 479 482 PF01048 0.682
MOD_GlcNHglycan 600 603 PF01048 0.460
MOD_GlcNHglycan 61 64 PF01048 0.647
MOD_GlcNHglycan 75 78 PF01048 0.786
MOD_GlcNHglycan 83 86 PF01048 0.724
MOD_GSK3_1 1 8 PF00069 0.756
MOD_GSK3_1 111 118 PF00069 0.742
MOD_GSK3_1 194 201 PF00069 0.750
MOD_GSK3_1 213 220 PF00069 0.727
MOD_GSK3_1 243 250 PF00069 0.689
MOD_GSK3_1 328 335 PF00069 0.470
MOD_GSK3_1 435 442 PF00069 0.724
MOD_GSK3_1 467 474 PF00069 0.665
MOD_GSK3_1 477 484 PF00069 0.663
MOD_GSK3_1 48 55 PF00069 0.787
MOD_GSK3_1 509 516 PF00069 0.622
MOD_GSK3_1 549 556 PF00069 0.623
MOD_GSK3_1 592 599 PF00069 0.689
MOD_GSK3_1 607 614 PF00069 0.367
MOD_GSK3_1 73 80 PF00069 0.760
MOD_GSK3_1 98 105 PF00069 0.728
MOD_N-GLC_1 143 148 PF02516 0.639
MOD_N-GLC_1 323 328 PF02516 0.418
MOD_NEK2_1 1 6 PF00069 0.706
MOD_NEK2_1 124 129 PF00069 0.670
MOD_NEK2_1 313 318 PF00069 0.470
MOD_NEK2_1 339 344 PF00069 0.470
MOD_NEK2_1 485 490 PF00069 0.692
MOD_NEK2_1 517 522 PF00069 0.472
MOD_NEK2_1 560 565 PF00069 0.501
MOD_NEK2_1 598 603 PF00069 0.530
MOD_NEK2_2 294 299 PF00069 0.418
MOD_NEK2_2 602 607 PF00069 0.546
MOD_NEK2_2 678 683 PF00069 0.498
MOD_PIKK_1 118 124 PF00454 0.699
MOD_PIKK_1 6 12 PF00454 0.771
MOD_PK_1 493 499 PF00069 0.660
MOD_PK_1 569 575 PF00069 0.540
MOD_PKA_1 189 195 PF00069 0.675
MOD_PKA_1 574 580 PF00069 0.594
MOD_PKA_2 124 130 PF00069 0.667
MOD_PKA_2 189 195 PF00069 0.791
MOD_PKA_2 243 249 PF00069 0.694
MOD_PKA_2 507 513 PF00069 0.658
MOD_PKA_2 59 65 PF00069 0.704
MOD_PKA_2 678 684 PF00069 0.499
MOD_Plk_1 457 463 PF00069 0.799
MOD_Plk_1 624 630 PF00069 0.599
MOD_Plk_4 25 31 PF00069 0.696
MOD_Plk_4 294 300 PF00069 0.457
MOD_Plk_4 313 319 PF00069 0.310
MOD_Plk_4 347 353 PF00069 0.422
MOD_Plk_4 527 533 PF00069 0.444
MOD_Plk_4 602 608 PF00069 0.547
MOD_ProDKin_1 220 226 PF00069 0.825
MOD_ProDKin_1 232 238 PF00069 0.685
MOD_ProDKin_1 247 253 PF00069 0.707
MOD_ProDKin_1 429 435 PF00069 0.723
MOD_ProDKin_1 447 453 PF00069 0.565
MOD_ProDKin_1 467 473 PF00069 0.678
MOD_ProDKin_1 590 596 PF00069 0.667
MOD_SUMO_for_1 384 387 PF00179 0.418
MOD_SUMO_rev_2 397 405 PF00179 0.397
TRG_DiLeu_BaEn_1 255 260 PF01217 0.470
TRG_DiLeu_BaLyEn_6 270 275 PF01217 0.392
TRG_ENDOCYTIC_2 159 162 PF00928 0.583
TRG_ENDOCYTIC_2 238 241 PF00928 0.655
TRG_ENDOCYTIC_2 561 564 PF00928 0.529
TRG_ER_diArg_1 188 190 PF00400 0.695
TRG_ER_diArg_1 411 413 PF00400 0.625
TRG_Pf-PMV_PEXEL_1 273 277 PF00026 0.483
TRG_Pf-PMV_PEXEL_1 515 519 PF00026 0.590
TRG_Pf-PMV_PEXEL_1 680 684 PF00026 0.625

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3S5H4Z6 Leishmania donovani 100% 100%
A4H3C9 Leishmania braziliensis 63% 100%
E9ACA6 Leishmania major 89% 100%
E9AJJ4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 76% 96%

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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