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: 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: E9B548
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.475 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.551 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.479 |
DEG_APCC_DBOX_1 | 528 | 536 | PF00400 | 0.554 |
DEG_APCC_KENBOX_2 | 396 | 400 | PF00400 | 0.601 |
DOC_CYCLIN_RxL_1 | 525 | 534 | PF00134 | 0.502 |
DOC_MAPK_gen_1 | 145 | 153 | PF00069 | 0.578 |
DOC_MAPK_MEF2A_6 | 495 | 504 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 92 | 100 | PF00069 | 0.411 |
DOC_PP1_RVXF_1 | 467 | 473 | PF00149 | 0.464 |
DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.523 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.395 |
DOC_USP7_UBL2_3 | 25 | 29 | PF12436 | 0.525 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.728 |
LIG_14-3-3_CanoR_1 | 404 | 414 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 457 | 461 | PF00244 | 0.490 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.617 |
LIG_CaM_IQ_9 | 247 | 262 | PF13499 | 0.501 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.561 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.564 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.386 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.560 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.422 |
LIG_Integrin_RGD_1 | 164 | 166 | PF01839 | 0.618 |
LIG_LIR_Gen_1 | 302 | 312 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 5 | 12 | PF02991 | 0.661 |
LIG_LIR_Gen_1 | 95 | 102 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 425 | 431 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 54 | 59 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.383 |
LIG_NRBOX | 335 | 341 | PF00104 | 0.617 |
LIG_PCNA_PIPBox_1 | 90 | 99 | PF02747 | 0.532 |
LIG_PDZ_Class_1 | 552 | 557 | PF00595 | 0.613 |
LIG_Pex14_2 | 122 | 126 | PF04695 | 0.544 |
LIG_SH2_GRB2like | 354 | 357 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 354 | 358 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 406 | 410 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.375 |
LIG_SUMO_SIM_anti_2 | 7 | 13 | PF11976 | 0.657 |
LIG_SUMO_SIM_par_1 | 295 | 300 | PF11976 | 0.648 |
LIG_SUMO_SIM_par_1 | 413 | 419 | PF11976 | 0.505 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.601 |
LIG_TRAF2_1 | 180 | 183 | PF00917 | 0.585 |
LIG_UBA3_1 | 196 | 202 | PF00899 | 0.566 |
LIG_UBA3_1 | 245 | 254 | PF00899 | 0.515 |
LIG_UBA3_1 | 274 | 279 | PF00899 | 0.623 |
LIG_WRC_WIRS_1 | 97 | 102 | PF05994 | 0.379 |
MOD_CDK_SPK_2 | 288 | 293 | PF00069 | 0.726 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.517 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.529 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.471 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.658 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.545 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.579 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.550 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.585 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.558 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.696 |
MOD_GlcNHglycan | 236 | 240 | PF01048 | 0.537 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.679 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.489 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.543 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.543 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.482 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.633 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.567 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.536 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.478 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.413 |
MOD_N-GLC_1 | 286 | 291 | PF02516 | 0.739 |
MOD_N-GLC_1 | 398 | 403 | PF02516 | 0.495 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.535 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.651 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.548 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.507 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.408 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.445 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.359 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.386 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.377 |
MOD_PIKK_1 | 106 | 112 | PF00454 | 0.605 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.607 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.609 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.495 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.596 |
MOD_PK_1 | 461 | 467 | PF00069 | 0.569 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.726 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.482 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.521 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.573 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.436 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.471 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.612 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.474 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.603 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.479 |
MOD_Plk_2-3 | 350 | 356 | PF00069 | 0.589 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.553 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.728 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.474 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.616 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.450 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.422 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.730 |
MOD_SUMO_for_1 | 228 | 231 | PF00179 | 0.507 |
MOD_SUMO_rev_2 | 163 | 171 | PF00179 | 0.599 |
MOD_SUMO_rev_2 | 218 | 224 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 367 | 374 | PF00179 | 0.555 |
MOD_SUMO_rev_2 | 447 | 456 | PF00179 | 0.589 |
TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.608 |
TRG_DiLeu_BaEn_1 | 304 | 309 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 35 | 40 | PF01217 | 0.418 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.375 |
TRG_ER_diArg_1 | 282 | 285 | PF00400 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 158 | 163 | PF00026 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 536 | 540 | PF00026 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 547 | 551 | PF00026 | 0.605 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P612 | Leptomonas seymouri | 70% | 98% |
A0A1X0P9R7 | Trypanosomatidae | 47% | 96% |
A0A3S7X860 | Leishmania donovani | 95% | 100% |
A0A422N8F5 | Trypanosoma rangeli | 47% | 96% |
A4HAX4 | Leishmania braziliensis | 84% | 100% |
A4IA33 | Leishmania infantum | 95% | 100% |
C9ZMJ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 95% |
Q4Q2T8 | Leishmania major | 96% | 100% |
V5BUY7 | Trypanosoma cruzi | 46% | 96% |