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 |
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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043228 | non-membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:1990904 | ribonucleoprotein complex | 2 | 10 |
GO:0035869 | ciliary transition zone | 2 | 2 |
Related structures:
AlphaFold database: A0A3Q8IGU1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 375 | 379 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.744 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.508 |
CLV_PCSK_FUR_1 | 75 | 79 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.740 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 403 | 405 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.534 |
CLV_Separin_Metazoa | 427 | 431 | PF03568 | 0.484 |
DEG_APCC_DBOX_1 | 373 | 381 | PF00400 | 0.477 |
DEG_APCC_DBOX_1 | 429 | 437 | PF00400 | 0.531 |
DEG_SPOP_SBC_1 | 449 | 453 | PF00917 | 0.494 |
DEG_SPOP_SBC_1 | 497 | 501 | PF00917 | 0.708 |
DOC_MAPK_gen_1 | 233 | 242 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 421 | 428 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 77 | 87 | PF00069 | 0.517 |
DOC_PP2B_LxvP_1 | 537 | 540 | PF13499 | 0.638 |
DOC_PP2B_LxvP_1 | 575 | 578 | PF13499 | 0.613 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.804 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.581 |
DOC_USP7_UBL2_3 | 399 | 403 | PF12436 | 0.585 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.688 |
LIG_14-3-3_CanoR_1 | 249 | 254 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 336 | 346 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 421 | 427 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 511 | 516 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 549 | 554 | PF00244 | 0.694 |
LIG_14-3-3_CterR_2 | 617 | 621 | PF00244 | 0.725 |
LIG_Actin_WH2_2 | 239 | 256 | PF00022 | 0.508 |
LIG_APCC_ABBA_1 | 106 | 111 | PF00400 | 0.479 |
LIG_BRCT_BRCA1_1 | 140 | 144 | PF00533 | 0.388 |
LIG_CtBP_PxDLS_1 | 492 | 496 | PF00389 | 0.523 |
LIG_EVH1_1 | 575 | 579 | PF00568 | 0.638 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.495 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.552 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.510 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.537 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.462 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.504 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.604 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.456 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.625 |
LIG_Integrin_RGD_1 | 133 | 135 | PF01839 | 0.415 |
LIG_LIR_Gen_1 | 211 | 220 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 44 | 55 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 211 | 216 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 565 | 571 | PF02991 | 0.722 |
LIG_LIR_Nem_3 | 86 | 91 | PF02991 | 0.458 |
LIG_LYPXL_SIV_4 | 344 | 352 | PF13949 | 0.593 |
LIG_NRBOX | 602 | 608 | PF00104 | 0.505 |
LIG_PCNA_yPIPBox_3 | 225 | 238 | PF02747 | 0.369 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.520 |
LIG_SH2_SRC | 171 | 174 | PF00017 | 0.509 |
LIG_SH2_SRC | 568 | 571 | PF00017 | 0.648 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 339 | 343 | PF00017 | 0.546 |
LIG_SH2_STAT3 | 339 | 342 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.602 |
LIG_SH3_1 | 444 | 450 | PF00018 | 0.621 |
LIG_SH3_2 | 536 | 541 | PF14604 | 0.599 |
LIG_SH3_2 | 593 | 598 | PF14604 | 0.578 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.665 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.636 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.594 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.720 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.781 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.642 |
LIG_SH3_3 | 533 | 539 | PF00018 | 0.691 |
LIG_SH3_3 | 541 | 547 | PF00018 | 0.771 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.641 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.648 |
LIG_SH3_3 | 588 | 594 | PF00018 | 0.651 |
LIG_SH3_CIN85_PxpxPR_1 | 536 | 541 | PF14604 | 0.527 |
LIG_SUMO_SIM_anti_2 | 361 | 367 | PF11976 | 0.609 |
LIG_SUMO_SIM_anti_2 | 425 | 430 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 485 | 490 | PF11976 | 0.634 |
LIG_SUMO_SIM_par_1 | 83 | 89 | PF11976 | 0.503 |
LIG_TRAF2_1 | 407 | 410 | PF00917 | 0.568 |
LIG_WRC_WIRS_1 | 373 | 378 | PF05994 | 0.542 |
LIG_WRC_WIRS_1 | 66 | 71 | PF05994 | 0.410 |
LIG_WW_3 | 538 | 542 | PF00397 | 0.527 |
MOD_CDK_SPxxK_3 | 8 | 15 | PF00069 | 0.555 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.382 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.476 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.378 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.524 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.531 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.762 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.514 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.562 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.742 |
MOD_DYRK1A_RPxSP_1 | 8 | 12 | PF00069 | 0.562 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.503 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.456 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.305 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.519 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.486 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.380 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.350 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.372 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.399 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.488 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.468 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.565 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.649 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.672 |
MOD_GlcNHglycan | 494 | 498 | PF01048 | 0.683 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.732 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.572 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.613 |
MOD_GlcNHglycan | 609 | 613 | PF01048 | 0.651 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.560 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.445 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.618 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.571 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.534 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.536 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.443 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.517 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.562 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.588 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.537 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.648 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.712 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.706 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.638 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.748 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.707 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.522 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.469 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.473 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.509 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.461 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.585 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.775 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.564 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.478 |
MOD_NEK2_2 | 83 | 88 | PF00069 | 0.406 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.450 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.629 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.540 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.612 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.617 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.565 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.646 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.739 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.473 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.677 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.497 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.445 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.489 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.516 |
MOD_Plk_1 | 493 | 499 | PF00069 | 0.800 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.478 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.516 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.730 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.456 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.620 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.640 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.719 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.651 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.686 |
MOD_SUMO_rev_2 | 24 | 29 | PF00179 | 0.484 |
MOD_SUMO_rev_2 | 416 | 423 | PF00179 | 0.490 |
TRG_DiLeu_BaEn_1 | 173 | 178 | PF01217 | 0.574 |
TRG_DiLeu_BaEn_1 | 358 | 363 | PF01217 | 0.531 |
TRG_DiLeu_BaLyEn_6 | 152 | 157 | PF01217 | 0.324 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 568 | 571 | PF00928 | 0.648 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.517 |
TRG_ER_diArg_1 | 115 | 117 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 429 | 431 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 617 | 619 | PF00400 | 0.751 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.638 |
TRG_Pf-PMV_PEXEL_1 | 168 | 173 | PF00026 | 0.309 |
TRG_Pf-PMV_PEXEL_1 | 357 | 361 | PF00026 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I367 | Leptomonas seymouri | 68% | 91% |
A0A1X0P0X2 | Trypanosomatidae | 39% | 94% |
A0A1X0P178 | Trypanosomatidae | 36% | 100% |
A0A3R7M637 | Trypanosoma rangeli | 34% | 100% |
A0A422N1N7 | Trypanosoma rangeli | 22% | 72% |
A4HLH8 | Leishmania braziliensis | 74% | 98% |
A4HLH9 | Leishmania braziliensis | 31% | 100% |
A4I8Y8 | Leishmania infantum | 99% | 100% |
E9B3V7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
E9B3V8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 71% |
Q4Q466 | Leishmania major | 29% | 73% |
Q4Q467 | Leishmania major | 92% | 100% |