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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X860
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.489 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.584 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.570 |
DEG_APCC_DBOX_1 | 528 | 536 | PF00400 | 0.572 |
DEG_APCC_KENBOX_2 | 396 | 400 | PF00400 | 0.633 |
DOC_CYCLIN_RxL_1 | 525 | 534 | PF00134 | 0.524 |
DOC_MAPK_gen_1 | 145 | 153 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 207 | 216 | PF00069 | 0.633 |
DOC_MAPK_MEF2A_6 | 495 | 504 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 92 | 100 | PF00069 | 0.420 |
DOC_PP1_RVXF_1 | 467 | 473 | PF00149 | 0.489 |
DOC_PP2B_LxvP_1 | 4 | 7 | PF13499 | 0.459 |
DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.521 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.585 |
DOC_USP7_UBL2_3 | 25 | 29 | PF12436 | 0.568 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.717 |
LIG_14-3-3_CanoR_1 | 404 | 414 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 457 | 461 | PF00244 | 0.479 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.621 |
LIG_BRCT_BRCA1_1 | 15 | 19 | PF00533 | 0.676 |
LIG_BRCT_BRCA1_1 | 43 | 47 | PF00533 | 0.361 |
LIG_BRCT_BRCA1_2 | 43 | 49 | PF00533 | 0.355 |
LIG_CaM_IQ_9 | 247 | 262 | PF13499 | 0.524 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.597 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.582 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.581 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.388 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.540 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.469 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.588 |
LIG_Integrin_RGD_1 | 164 | 166 | PF01839 | 0.635 |
LIG_LIR_Gen_1 | 302 | 312 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 5 | 12 | PF02991 | 0.672 |
LIG_LIR_Gen_1 | 65 | 75 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 95 | 102 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 425 | 431 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 54 | 59 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 65 | 71 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.395 |
LIG_NRBOX | 335 | 341 | PF00104 | 0.639 |
LIG_PCNA_PIPBox_1 | 90 | 99 | PF02747 | 0.537 |
LIG_PCNA_yPIPBox_3 | 260 | 274 | PF02747 | 0.621 |
LIG_PDZ_Class_2 | 552 | 557 | PF00595 | 0.480 |
LIG_Pex14_2 | 122 | 126 | PF04695 | 0.546 |
LIG_Pex14_2 | 43 | 47 | PF04695 | 0.361 |
LIG_SH2_GRB2like | 354 | 357 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 354 | 358 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 406 | 410 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.389 |
LIG_SUMO_SIM_par_1 | 295 | 300 | PF11976 | 0.652 |
LIG_SUMO_SIM_par_1 | 413 | 419 | PF11976 | 0.525 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.607 |
LIG_TRAF2_1 | 180 | 183 | PF00917 | 0.595 |
LIG_UBA3_1 | 196 | 202 | PF00899 | 0.581 |
LIG_UBA3_1 | 245 | 254 | PF00899 | 0.537 |
LIG_UBA3_1 | 274 | 279 | PF00899 | 0.645 |
LIG_WRC_WIRS_1 | 40 | 45 | PF05994 | 0.401 |
LIG_WRC_WIRS_1 | 68 | 73 | PF05994 | 0.483 |
LIG_WRC_WIRS_1 | 97 | 102 | PF05994 | 0.392 |
MOD_CDK_SPK_2 | 288 | 293 | PF00069 | 0.742 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.507 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.539 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.473 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.509 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.487 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.481 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.601 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.716 |
MOD_GlcNHglycan | 236 | 240 | PF01048 | 0.551 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.696 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.517 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.567 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.635 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.589 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.543 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.500 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.426 |
MOD_N-GLC_1 | 286 | 291 | PF02516 | 0.770 |
MOD_N-GLC_1 | 398 | 403 | PF02516 | 0.519 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.528 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.568 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.528 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.436 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.469 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.366 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.397 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.383 |
MOD_PIKK_1 | 106 | 112 | PF00454 | 0.612 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.608 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.633 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.523 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.613 |
MOD_PK_1 | 461 | 467 | PF00069 | 0.592 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.737 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.507 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.550 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.445 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.493 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.620 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.506 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.478 |
MOD_Plk_2-3 | 350 | 356 | PF00069 | 0.611 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.555 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.737 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.506 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.447 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.651 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.433 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.720 |
MOD_SUMO_for_1 | 228 | 231 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 163 | 171 | PF00179 | 0.589 |
MOD_SUMO_rev_2 | 218 | 224 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 367 | 374 | PF00179 | 0.581 |
MOD_SUMO_rev_2 | 448 | 456 | PF00179 | 0.610 |
MOD_SUMO_rev_2 | 52 | 59 | PF00179 | 0.465 |
TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.621 |
TRG_DiLeu_BaEn_1 | 304 | 309 | PF01217 | 0.524 |
TRG_DiLeu_BaEn_1 | 442 | 447 | PF01217 | 0.482 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 536 | 540 | PF00026 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 547 | 551 | PF00026 | 0.610 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P612 | Leptomonas seymouri | 70% | 98% |
A0A1X0P9R7 | Trypanosomatidae | 47% | 96% |
A0A422N8F5 | Trypanosoma rangeli | 48% | 96% |
A4HAX4 | Leishmania braziliensis | 84% | 100% |
A4IA33 | Leishmania infantum | 100% | 100% |
C9ZMJ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 95% |
E9B548 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4Q2T8 | Leishmania major | 97% | 100% |
V5BUY7 | Trypanosoma cruzi | 47% | 96% |