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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030684 | preribosome | 3 | 1 |
GO:0030687 | preribosome, large subunit precursor | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
GO:0005634 | nucleus | 5 | 2 |
GO:0005694 | chromosome | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A0A3Q8IGI0
Term | Name | Level | Count |
---|---|---|---|
GO:0000027 | ribosomal large subunit assembly | 7 | 1 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006260 | DNA replication | 5 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 3 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 3 |
GO:0019843 | rRNA binding | 5 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
GO:0003677 | DNA binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 224 | 228 | PF00656 | 0.564 |
CLV_C14_Caspase3-7 | 24 | 28 | PF00656 | 0.562 |
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.464 |
CLV_C14_Caspase3-7 | 429 | 433 | PF00656 | 0.618 |
CLV_C14_Caspase3-7 | 440 | 444 | PF00656 | 0.697 |
CLV_C14_Caspase3-7 | 458 | 462 | PF00656 | 0.704 |
CLV_C14_Caspase3-7 | 83 | 87 | PF00656 | 0.412 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.620 |
CLV_PCSK_FUR_1 | 495 | 499 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.685 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 494 | 496 | PF00082 | 0.670 |
CLV_PCSK_PC1ET2_1 | 497 | 499 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 500 | 502 | PF00082 | 0.685 |
CLV_PCSK_PC1ET2_1 | 506 | 508 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 512 | 514 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 521 | 525 | PF00082 | 0.583 |
DOC_CYCLIN_RxL_1 | 278 | 288 | PF00134 | 0.546 |
DOC_CYCLIN_RxL_1 | 362 | 372 | PF00134 | 0.528 |
DOC_CYCLIN_yCln2_LP_2 | 239 | 245 | PF00134 | 0.420 |
DOC_CYCLIN_yCln2_LP_2 | 57 | 63 | PF00134 | 0.523 |
DOC_MAPK_DCC_7 | 96 | 104 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 29 | 37 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 72 | 79 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 96 | 104 | PF00069 | 0.452 |
DOC_PP1_RVXF_1 | 365 | 371 | PF00149 | 0.528 |
DOC_PP1_RVXF_1 | 91 | 98 | PF00149 | 0.482 |
DOC_PP2B_LxvP_1 | 283 | 286 | PF13499 | 0.570 |
DOC_PP2B_LxvP_1 | 38 | 41 | PF13499 | 0.482 |
DOC_PP2B_LxvP_1 | 57 | 60 | PF13499 | 0.523 |
DOC_PP4_FxxP_1 | 97 | 100 | PF00568 | 0.438 |
DOC_SPAK_OSR1_1 | 96 | 100 | PF12202 | 0.438 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.463 |
DOC_USP7_UBL2_3 | 17 | 21 | PF12436 | 0.631 |
DOC_USP7_UBL2_3 | 240 | 244 | PF12436 | 0.487 |
DOC_USP7_UBL2_3 | 313 | 317 | PF12436 | 0.465 |
DOC_USP7_UBL2_3 | 398 | 402 | PF12436 | 0.517 |
DOC_USP7_UBL2_3 | 42 | 46 | PF12436 | 0.606 |
DOC_USP7_UBL2_3 | 481 | 485 | PF12436 | 0.659 |
DOC_USP7_UBL2_3 | 488 | 492 | PF12436 | 0.545 |
DOC_USP7_UBL2_3 | 500 | 504 | PF12436 | 0.625 |
DOC_USP7_UBL2_3 | 506 | 510 | PF12436 | 0.551 |
DOC_USP7_UBL2_3 | 512 | 516 | PF12436 | 0.631 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.491 |
LIG_14-3-3_CanoR_1 | 246 | 251 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 80 | 90 | PF00244 | 0.488 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.638 |
LIG_BRCT_BRCA1_1 | 93 | 97 | PF00533 | 0.452 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.536 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.656 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.599 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.499 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.494 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.591 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.466 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.513 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.382 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.657 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.452 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.513 |
LIG_LIR_Apic_2 | 94 | 100 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 165 | 174 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 183 | 189 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 247 | 258 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 356 | 365 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 165 | 169 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.215 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.471 |
LIG_MYND_1 | 294 | 298 | PF01753 | 0.537 |
LIG_PCNA_PIPBox_1 | 337 | 346 | PF02747 | 0.484 |
LIG_PDZ_Class_1 | 522 | 527 | PF00595 | 0.566 |
LIG_PTB_Apo_2 | 352 | 359 | PF02174 | 0.528 |
LIG_PTB_Apo_2 | 45 | 52 | PF02174 | 0.597 |
LIG_PTB_Phospho_1 | 45 | 51 | PF10480 | 0.597 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.338 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.344 |
LIG_SH2_CRK | 321 | 325 | PF00017 | 0.483 |
LIG_SH2_CRK | 328 | 332 | PF00017 | 0.481 |
LIG_SH2_PTP2 | 234 | 237 | PF00017 | 0.335 |
LIG_SH2_SRC | 457 | 460 | PF00017 | 0.644 |
LIG_SH2_SRC | 51 | 54 | PF00017 | 0.518 |
LIG_SH2_STAT3 | 127 | 130 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.218 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.582 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.479 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.532 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.565 |
LIG_SH3_4 | 17 | 24 | PF00018 | 0.657 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.630 |
LIG_TRAF2_1 | 409 | 412 | PF00917 | 0.528 |
LIG_TRAF2_1 | 446 | 449 | PF00917 | 0.674 |
LIG_TYR_ITSM | 246 | 253 | PF00017 | 0.454 |
LIG_UBA3_1 | 37 | 42 | PF00899 | 0.469 |
LIG_UBA3_1 | 416 | 425 | PF00899 | 0.455 |
LIG_WRC_WIRS_1 | 163 | 168 | PF05994 | 0.477 |
LIG_WRC_WIRS_1 | 200 | 205 | PF05994 | 0.410 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.358 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.547 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.716 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.463 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.545 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.459 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.383 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.739 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.510 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.529 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.372 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.488 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.400 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.255 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.282 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.341 |
MOD_GlcNHglycan | 464 | 470 | PF01048 | 0.714 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.271 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.245 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.510 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.466 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.387 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.470 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.475 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.547 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.480 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.424 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.562 |
MOD_N-GLC_2 | 101 | 103 | PF02516 | 0.450 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.500 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.537 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.457 |
MOD_PIKK_1 | 272 | 278 | PF00454 | 0.419 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.516 |
MOD_PKA_1 | 193 | 199 | PF00069 | 0.472 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.408 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.379 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.512 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.548 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.458 |
MOD_Plk_2-3 | 19 | 25 | PF00069 | 0.631 |
MOD_Plk_2-3 | 443 | 449 | PF00069 | 0.736 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.488 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.453 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.517 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.497 |
MOD_SUMO_for_1 | 16 | 19 | PF00179 | 0.622 |
MOD_SUMO_for_1 | 20 | 23 | PF00179 | 0.625 |
MOD_SUMO_for_1 | 409 | 412 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 14 | 22 | PF00179 | 0.610 |
MOD_SUMO_rev_2 | 266 | 275 | PF00179 | 0.440 |
MOD_SUMO_rev_2 | 435 | 444 | PF00179 | 0.564 |
MOD_SUMO_rev_2 | 477 | 487 | PF00179 | 0.716 |
TRG_DiLeu_BaEn_1 | 412 | 417 | PF01217 | 0.438 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.473 |
TRG_NLS_MonoCore_2 | 477 | 482 | PF00514 | 0.743 |
TRG_NLS_MonoExtC_3 | 477 | 482 | PF00514 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 367 | 372 | PF00026 | 0.294 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PG07 | Leptomonas seymouri | 80% | 100% |
A0A0S4IUW8 | Bodo saltans | 31% | 100% |
A0A1X0P6K5 | Trypanosomatidae | 43% | 90% |
A0A422P127 | Trypanosoma rangeli | 46% | 94% |
A4HK02 | Leishmania braziliensis | 87% | 100% |
A4I7I5 | Leishmania infantum | 100% | 100% |
D0A088 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 95% |
E9B2E2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
O01683 | Caenorhabditis elegans | 24% | 76% |
O04235 | Vicia faba | 22% | 82% |
O94529 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 100% |
P0CR74 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 23% | 90% |
P0CR75 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 23% | 90% |
P41848 | Caenorhabditis elegans | 25% | 76% |
Q04636 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 95% |
Q04678 | Gallus gallus | 22% | 75% |
Q04931 | Rattus norvegicus | 22% | 74% |
Q05153 | Arabidopsis thaliana | 20% | 82% |
Q05344 | Drosophila melanogaster | 24% | 73% |
Q08943 | Mus musculus | 22% | 74% |
Q08945 | Homo sapiens | 23% | 74% |
Q293F6 | Drosophila pseudoobscura pseudoobscura | 24% | 72% |
Q2USL9 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 22% | 91% |
Q39601 | Catharanthus roseus | 22% | 82% |
Q4Q5R4 | Leishmania major | 95% | 100% |
Q4WGK6 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 22% | 92% |
Q5ALL8 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 23% | 98% |
Q5AYE3 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 24% | 92% |
Q6CWD7 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 23% | 95% |
Q6FKI2 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 24% | 97% |
Q756X6 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 25% | 97% |
Q9LEF5 | Zea mays | 21% | 82% |
Q9LGR0 | Oryza sativa subsp. japonica | 25% | 82% |
Q9W602 | Xenopus laevis | 22% | 76% |