Intracellular protein trafficking, Soluble NSF attachment , SNAP
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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031201 | SNARE complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HRM8
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 |
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 |
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 |
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% |