Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | 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: A4H3C9
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 | 495 | 499 | PF00656 | 0.588 |
CLV_C14_Caspase3-7 | 524 | 528 | PF00656 | 0.500 |
CLV_C14_Caspase3-7 | 615 | 619 | PF00656 | 0.396 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 693 | 695 | PF00675 | 0.585 |
CLV_PCSK_FUR_1 | 429 | 433 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 693 | 695 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.674 |
CLV_PCSK_PC1ET2_1 | 431 | 433 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 630 | 634 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 652 | 656 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 694 | 698 | PF00082 | 0.577 |
DEG_APCC_DBOX_1 | 529 | 537 | PF00400 | 0.456 |
DEG_APCC_KENBOX_2 | 645 | 649 | PF00400 | 0.505 |
DEG_SPOP_SBC_1 | 246 | 250 | PF00917 | 0.520 |
DOC_CYCLIN_RxL_1 | 321 | 330 | PF00134 | 0.420 |
DOC_CYCLIN_RxL_1 | 562 | 571 | PF00134 | 0.428 |
DOC_CYCLIN_RxL_1 | 690 | 701 | PF00134 | 0.570 |
DOC_MAPK_gen_1 | 530 | 537 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 354 | 362 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 530 | 537 | PF00069 | 0.457 |
DOC_PP1_RVXF_1 | 301 | 308 | PF00149 | 0.420 |
DOC_PP2B_LxvP_1 | 13 | 16 | PF13499 | 0.568 |
DOC_PP2B_LxvP_1 | 476 | 479 | PF13499 | 0.538 |
DOC_PP2B_LxvP_1 | 559 | 562 | PF13499 | 0.377 |
DOC_PP2B_PxIxI_1 | 357 | 363 | PF00149 | 0.420 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.251 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 600 | 604 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 613 | 617 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.675 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 202 | 208 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 226 | 231 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 279 | 288 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 334 | 343 | PF00244 | 0.251 |
LIG_14-3-3_CanoR_1 | 500 | 506 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 516 | 522 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 523 | 531 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 577 | 583 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 62 | 68 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 659 | 664 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 693 | 697 | PF00244 | 0.451 |
LIG_Actin_WH2_2 | 339 | 356 | PF00022 | 0.420 |
LIG_APCC_ABBA_1 | 410 | 415 | PF00400 | 0.420 |
LIG_BIR_III_2 | 146 | 150 | PF00653 | 0.547 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.653 |
LIG_BRCT_BRCA1_1 | 503 | 507 | PF00533 | 0.684 |
LIG_deltaCOP1_diTrp_1 | 297 | 306 | PF00928 | 0.490 |
LIG_deltaCOP1_diTrp_1 | 76 | 84 | PF00928 | 0.540 |
LIG_eIF4E_1 | 626 | 632 | PF01652 | 0.309 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.659 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.420 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.611 |
LIG_FHA_1 | 562 | 568 | PF00498 | 0.463 |
LIG_FHA_1 | 569 | 575 | PF00498 | 0.405 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.406 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.467 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.674 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.628 |
LIG_LIR_Apic_2 | 204 | 208 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 629 | 639 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 695 | 704 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 564 | 569 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 629 | 635 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 672 | 676 | PF02991 | 0.450 |
LIG_LYPXL_SIV_4 | 280 | 288 | PF13949 | 0.471 |
LIG_MYND_1 | 11 | 15 | PF01753 | 0.568 |
LIG_NRBOX | 532 | 538 | PF00104 | 0.449 |
LIG_PCNA_yPIPBox_3 | 23 | 34 | PF02747 | 0.552 |
LIG_Pex14_1 | 205 | 209 | PF04695 | 0.546 |
LIG_PTB_Apo_2 | 330 | 337 | PF02174 | 0.420 |
LIG_PTB_Apo_2 | 83 | 90 | PF02174 | 0.534 |
LIG_SH2_CRK | 569 | 573 | PF00017 | 0.438 |
LIG_SH2_NCK_1 | 281 | 285 | PF00017 | 0.464 |
LIG_SH2_SRC | 543 | 546 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 621 | 624 | PF00017 | 0.484 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.670 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.501 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.662 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.602 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.496 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.251 |
LIG_SH3_3 | 502 | 508 | PF00018 | 0.616 |
LIG_SUMO_SIM_anti_2 | 63 | 69 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 487 | 496 | PF11976 | 0.535 |
LIG_SUMO_SIM_par_1 | 532 | 538 | PF11976 | 0.419 |
LIG_TYR_ITIM | 567 | 572 | PF00017 | 0.439 |
LIG_WW_1 | 512 | 515 | PF00397 | 0.641 |
MOD_CDK_SPK_2 | 434 | 439 | PF00069 | 0.487 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.703 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.681 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.571 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.551 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.596 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.489 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.583 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.421 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.466 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.251 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.630 |
MOD_CK2_1 | 692 | 698 | PF00069 | 0.444 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.604 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.738 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.610 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.746 |
MOD_GlcNHglycan | 239 | 243 | PF01048 | 0.625 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.520 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.738 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.550 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.711 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.711 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.664 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.565 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.675 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.420 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.643 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.607 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.714 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.567 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.561 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.600 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.567 |
MOD_N-GLC_2 | 86 | 88 | PF02516 | 0.535 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.536 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.608 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.570 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.420 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.420 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.568 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.447 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.508 |
MOD_NEK2_2 | 621 | 626 | PF00069 | 0.442 |
MOD_NEK2_2 | 692 | 697 | PF00069 | 0.444 |
MOD_PIKK_1 | 413 | 419 | PF00454 | 0.251 |
MOD_PK_1 | 226 | 232 | PF00069 | 0.560 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.734 |
MOD_PKA_2 | 515 | 521 | PF00069 | 0.601 |
MOD_PKA_2 | 600 | 606 | PF00069 | 0.550 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.642 |
MOD_PKA_2 | 692 | 698 | PF00069 | 0.444 |
MOD_Plk_1 | 463 | 469 | PF00069 | 0.737 |
MOD_Plk_1 | 638 | 644 | PF00069 | 0.538 |
MOD_Plk_2-3 | 117 | 123 | PF00069 | 0.559 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.674 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.260 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.536 |
MOD_Plk_4 | 621 | 627 | PF00069 | 0.443 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.546 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.770 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.625 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.585 |
MOD_SUMO_for_1 | 135 | 138 | PF00179 | 0.559 |
MOD_SUMO_rev_2 | 393 | 401 | PF00179 | 0.265 |
TRG_DiLeu_BaEn_1 | 269 | 274 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 127 | 132 | PF01217 | 0.593 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.613 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.475 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.561 |
TRG_Pf-PMV_PEXEL_1 | 523 | 527 | PF00026 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 694 | 698 | PF00026 | 0.572 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H4Z6 | Leishmania donovani | 63% | 100% |
A4HRM8 | Leishmania infantum | 63% | 100% |
E9ACA6 | Leishmania major | 61% | 100% |
E9AJJ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |