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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 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 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9B428
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 1 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 1 |
GO:0042254 | ribosome biogenesis | 5 | 1 |
GO:0044085 | cellular component biogenesis | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 175 | 179 | PF00656 | 0.511 |
CLV_C14_Caspase3-7 | 220 | 224 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.588 |
CLV_C14_Caspase3-7 | 8 | 12 | PF00656 | 0.626 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.379 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.575 |
CLV_PCSK_PC1ET2_1 | 6 | 8 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.468 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.540 |
DEG_APCC_DBOX_1 | 199 | 207 | PF00400 | 0.508 |
DEG_APCC_DBOX_1 | 505 | 513 | PF00400 | 0.421 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.587 |
DEG_SPOP_SBC_1 | 382 | 386 | PF00917 | 0.394 |
DOC_CKS1_1 | 335 | 340 | PF01111 | 0.373 |
DOC_CKS1_1 | 469 | 474 | PF01111 | 0.429 |
DOC_CYCLIN_yClb1_LxF_4 | 145 | 150 | PF00134 | 0.579 |
DOC_MAPK_gen_1 | 328 | 335 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 421 | 430 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 444 | 453 | PF00069 | 0.344 |
DOC_MAPK_gen_1 | 482 | 490 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 162 | 170 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 200 | 208 | PF00069 | 0.500 |
DOC_PP1_RVXF_1 | 145 | 151 | PF00149 | 0.365 |
DOC_PP1_RVXF_1 | 425 | 431 | PF00149 | 0.353 |
DOC_PP1_RVXF_1 | 99 | 106 | PF00149 | 0.523 |
DOC_PP4_FxxP_1 | 335 | 338 | PF00568 | 0.355 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.687 |
DOC_USP7_UBL2_3 | 2 | 6 | PF12436 | 0.613 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.366 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.276 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.486 |
LIG_14-3-3_CanoR_1 | 182 | 190 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 302 | 310 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 37 | 44 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 378 | 387 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 446 | 453 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 506 | 510 | PF00244 | 0.400 |
LIG_APCC_ABBA_1 | 490 | 495 | PF00400 | 0.338 |
LIG_BRCT_BRCA1_1 | 101 | 105 | PF00533 | 0.675 |
LIG_BRCT_BRCA1_1 | 486 | 490 | PF00533 | 0.292 |
LIG_CaM_NSCaTE_8 | 128 | 135 | PF13499 | 0.539 |
LIG_eIF4E_1 | 568 | 574 | PF01652 | 0.296 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.513 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.483 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.513 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.405 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.353 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.295 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.292 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.306 |
LIG_FHA_2 | 564 | 570 | PF00498 | 0.441 |
LIG_Integrin_RGD_1 | 129 | 131 | PF01839 | 0.597 |
LIG_LIR_Gen_1 | 169 | 175 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 82 | 91 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 163 | 168 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 169 | 173 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 565 | 571 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.470 |
LIG_LYPXL_yS_3 | 165 | 168 | PF13949 | 0.409 |
LIG_PCNA_PIPBox_1 | 522 | 531 | PF02747 | 0.537 |
LIG_PCNA_yPIPBox_3 | 494 | 506 | PF02747 | 0.423 |
LIG_PCNA_yPIPBox_3 | 516 | 529 | PF02747 | 0.522 |
LIG_PTB_Apo_2 | 149 | 156 | PF02174 | 0.409 |
LIG_PTB_Phospho_1 | 149 | 155 | PF10480 | 0.409 |
LIG_REV1ctd_RIR_1 | 156 | 165 | PF16727 | 0.409 |
LIG_SH2_NCK_1 | 216 | 220 | PF00017 | 0.630 |
LIG_SH2_STAP1 | 155 | 159 | PF00017 | 0.423 |
LIG_SH2_STAT3 | 536 | 539 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.460 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.303 |
LIG_SUMO_SIM_anti_2 | 202 | 207 | PF11976 | 0.483 |
LIG_SUMO_SIM_anti_2 | 495 | 504 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 280 | 288 | PF11976 | 0.329 |
LIG_SUMO_SIM_par_1 | 413 | 420 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 495 | 504 | PF11976 | 0.312 |
LIG_TRAF2_1 | 392 | 395 | PF00917 | 0.313 |
LIG_UBA3_1 | 573 | 580 | PF00899 | 0.451 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.511 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.373 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.405 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.330 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.700 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.686 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.340 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.437 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.301 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.546 |
MOD_CK2_1 | 563 | 569 | PF00069 | 0.440 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.501 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.499 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.266 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.244 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.310 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.538 |
MOD_GlcNHglycan | 91 | 95 | PF01048 | 0.600 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.723 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.510 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.373 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.180 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.361 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.297 |
MOD_LATS_1 | 481 | 487 | PF00433 | 0.408 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.220 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.672 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.458 |
MOD_N-GLC_1 | 493 | 498 | PF02516 | 0.333 |
MOD_N-GLC_2 | 210 | 212 | PF02516 | 0.209 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.409 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.420 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.289 |
MOD_NEK2_2 | 364 | 369 | PF00069 | 0.362 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.409 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.503 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.366 |
MOD_PKA_1 | 6 | 12 | PF00069 | 0.665 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.406 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.667 |
MOD_PKB_1 | 35 | 43 | PF00069 | 0.443 |
MOD_PKB_1 | 444 | 452 | PF00069 | 0.394 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.391 |
MOD_Plk_1 | 493 | 499 | PF00069 | 0.346 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.630 |
MOD_Plk_1 | 510 | 516 | PF00069 | 0.257 |
MOD_Plk_2-3 | 217 | 223 | PF00069 | 0.507 |
MOD_Plk_2-3 | 232 | 238 | PF00069 | 0.563 |
MOD_Plk_2-3 | 50 | 56 | PF00069 | 0.584 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.521 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.412 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.349 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.290 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.315 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.279 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.483 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.372 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.279 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.327 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.478 |
MOD_SUMO_for_1 | 146 | 149 | PF00179 | 0.549 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 568 | 571 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.454 |
TRG_ER_diArg_1 | 34 | 37 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 466 | 468 | PF00400 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 302 | 306 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 37 | 41 | PF00026 | 0.678 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P833 | Leptomonas seymouri | 82% | 100% |
A0A0N0P8W9 | Leptomonas seymouri | 23% | 87% |
A0A0S4IIU6 | Bodo saltans | 63% | 97% |
A0A1X0P3N3 | Trypanosomatidae | 63% | 100% |
A0A3S7X390 | Leishmania donovani | 23% | 90% |
A0A3S7X6T4 | Leishmania donovani | 95% | 100% |
A0A422N600 | Trypanosoma rangeli | 61% | 100% |
A4HLQ3 | Leishmania braziliensis | 88% | 100% |
A4I5C6 | Leishmania infantum | 23% | 90% |
A4I953 | Leishmania infantum | 95% | 100% |
D0A6C1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
E9B0M4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 90% |
O22466 | Solanum lycopersicum | 23% | 100% |
O22468 | Arabidopsis thaliana | 23% | 100% |
O22469 | Arabidopsis thaliana | 23% | 100% |
P0CS36 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 22% | 100% |
P0CS37 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 22% | 100% |
P90916 | Caenorhabditis elegans | 25% | 100% |
Q04225 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
Q1JQD2 | Bos taurus | 31% | 100% |
Q2UA71 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 24% | 100% |
Q4P553 | Ustilago maydis (strain 521 / FGSC 9021) | 25% | 100% |
Q4Q3Z6 | Leishmania major | 94% | 100% |
Q4Q7K8 | Leishmania major | 23% | 90% |
Q4WEI5 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 24% | 100% |
Q54ED4 | Dictyostelium discoideum | 33% | 100% |
Q54SD4 | Dictyostelium discoideum | 25% | 100% |
Q5XI13 | Rattus norvegicus | 32% | 100% |
Q61Y48 | Caenorhabditis briggsae | 22% | 100% |
Q7S7N3 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 22% | 100% |
Q810D6 | Mus musculus | 32% | 100% |
Q9BQ67 | Homo sapiens | 33% | 100% |
Q9I8G9 | Gallus gallus | 23% | 100% |
Q9P783 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
Q9SU78 | Arabidopsis thaliana | 22% | 100% |
Q9ZUN8 | Arabidopsis thaliana | 33% | 100% |
V5BPB2 | Trypanosoma cruzi | 56% | 94% |