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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 7 |
GO:0005813 | centrosome | 3 | 2 |
GO:0005815 | microtubule organizing center | 2 | 2 |
GO:0036064 | ciliary basal body | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9AE54
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 7 |
GO:0019222 | regulation of metabolic process | 3 | 7 |
GO:0030865 | cortical cytoskeleton organization | 6 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 7 |
GO:0035303 | regulation of dephosphorylation | 7 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0005509 | calcium ion binding | 5 | 6 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 335 | 339 | PF00656 | 0.453 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.667 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.435 |
DOC_CKS1_1 | 525 | 530 | PF01111 | 0.363 |
DOC_CYCLIN_RxL_1 | 374 | 384 | PF00134 | 0.334 |
DOC_CYCLIN_yCln2_LP_2 | 150 | 153 | PF00134 | 0.471 |
DOC_CYCLIN_yCln2_LP_2 | 194 | 200 | PF00134 | 0.629 |
DOC_MAPK_gen_1 | 60 | 68 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 291 | 298 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 93 | 101 | PF00069 | 0.377 |
DOC_PP1_RVXF_1 | 375 | 382 | PF00149 | 0.331 |
DOC_PP1_RVXF_1 | 492 | 499 | PF00149 | 0.335 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.537 |
DOC_PP2B_LxvP_1 | 194 | 197 | PF13499 | 0.690 |
DOC_PP2B_LxvP_1 | 547 | 550 | PF13499 | 0.393 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.379 |
DOC_USP7_UBL2_3 | 102 | 106 | PF12436 | 0.410 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 465 | 470 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 524 | 529 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.376 |
LIG_14-3-3_CanoR_1 | 123 | 129 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 195 | 201 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 202 | 211 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 229 | 234 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 340 | 346 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 392 | 397 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 60 | 68 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 86 | 95 | PF00244 | 0.415 |
LIG_Actin_RPEL_3 | 571 | 590 | PF02755 | 0.349 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.656 |
LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.515 |
LIG_CtBP_PxDLS_1 | 197 | 201 | PF00389 | 0.605 |
LIG_deltaCOP1_diTrp_1 | 39 | 46 | PF00928 | 0.553 |
LIG_eIF4E_1 | 429 | 435 | PF01652 | 0.438 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.547 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.663 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.353 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.389 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.508 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.494 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.378 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.474 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.578 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.512 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.471 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.460 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.434 |
LIG_FHA_2 | 570 | 576 | PF00498 | 0.368 |
LIG_LIR_Gen_1 | 129 | 138 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 232 | 240 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 403 | 411 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 558 | 566 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 403 | 408 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 489 | 495 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 558 | 563 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 594 | 598 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.411 |
LIG_NRBOX | 113 | 119 | PF00104 | 0.400 |
LIG_NRP_CendR_1 | 601 | 604 | PF00754 | 0.471 |
LIG_PALB2_WD40_1 | 415 | 423 | PF16756 | 0.436 |
LIG_PCNA_yPIPBox_3 | 270 | 282 | PF02747 | 0.576 |
LIG_PTB_Apo_2 | 277 | 284 | PF02174 | 0.555 |
LIG_PTB_Apo_2 | 529 | 536 | PF02174 | 0.356 |
LIG_PTB_Phospho_1 | 277 | 283 | PF10480 | 0.556 |
LIG_REV1ctd_RIR_1 | 532 | 540 | PF16727 | 0.353 |
LIG_SH2_GRB2like | 598 | 601 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.393 |
LIG_SH2_STAT3 | 146 | 149 | PF00017 | 0.495 |
LIG_SH2_STAT3 | 243 | 246 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.409 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.622 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.422 |
LIG_SH3_3 | 522 | 528 | PF00018 | 0.371 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.376 |
LIG_SUMO_SIM_par_1 | 10 | 16 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 497 | 503 | PF11976 | 0.326 |
LIG_TRAF2_1 | 23 | 26 | PF00917 | 0.507 |
LIG_TRAF2_1 | 37 | 40 | PF00917 | 0.451 |
LIG_WRC_WIRS_1 | 19 | 24 | PF05994 | 0.531 |
LIG_WRC_WIRS_1 | 314 | 319 | PF05994 | 0.366 |
LIG_WW_3 | 288 | 292 | PF00397 | 0.390 |
MOD_CDC14_SPxK_1 | 192 | 195 | PF00782 | 0.557 |
MOD_CDK_SPxK_1 | 189 | 195 | PF00069 | 0.560 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.722 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.605 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.669 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.633 |
MOD_CK1_1 | 551 | 557 | PF00069 | 0.352 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.355 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.479 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.639 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.477 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.396 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.440 |
MOD_CK2_1 | 569 | 575 | PF00069 | 0.378 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.489 |
MOD_GlcNHglycan | 180 | 184 | PF01048 | 0.770 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.765 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.576 |
MOD_GlcNHglycan | 250 | 254 | PF01048 | 0.690 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.385 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.781 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.588 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.606 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.361 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.401 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.433 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.376 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.424 |
MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.638 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.634 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.564 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.544 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.406 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.494 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.406 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.356 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.457 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.406 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.399 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.443 |
MOD_NEK2_2 | 469 | 474 | PF00069 | 0.398 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.536 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.530 |
MOD_PIKK_1 | 413 | 419 | PF00454 | 0.411 |
MOD_PIKK_1 | 422 | 428 | PF00454 | 0.339 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.377 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.426 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.396 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.383 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.354 |
MOD_PKA_2 | 551 | 557 | PF00069 | 0.372 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.481 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.475 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.469 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.575 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.545 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.352 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.363 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.525 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.290 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.375 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.372 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.406 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.338 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.508 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.704 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.539 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.615 |
MOD_ProDKin_1 | 465 | 471 | PF00069 | 0.370 |
MOD_ProDKin_1 | 524 | 530 | PF00069 | 0.364 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.368 |
MOD_SUMO_for_1 | 324 | 327 | PF00179 | 0.343 |
TRG_DiLeu_BaEn_1 | 480 | 485 | PF01217 | 0.418 |
TRG_DiLeu_BaEn_1 | 558 | 563 | PF01217 | 0.359 |
TRG_DiLeu_BaEn_1 | 83 | 88 | PF01217 | 0.468 |
TRG_DiLeu_LyEn_5 | 83 | 88 | PF01217 | 0.468 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 492 | 495 | PF00928 | 0.347 |
TRG_ER_diArg_1 | 377 | 379 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 377 | 382 | PF00026 | 0.337 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.551 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC66 | Leptomonas seymouri | 68% | 96% |
A0A3Q8IFG2 | Leishmania donovani | 95% | 100% |
A4HHJ3 | Leishmania braziliensis | 87% | 99% |
A4I4Q1 | Leishmania infantum | 95% | 100% |
E9ALN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |