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: A4HK02
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 | 0.535 |
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.453 |
CLV_C14_Caspase3-7 | 429 | 433 | PF00656 | 0.613 |
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.747 |
CLV_C14_Caspase3-7 | 529 | 533 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.547 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 481 | 483 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 504 | 506 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.231 |
DEG_APCC_DBOX_1 | 427 | 435 | PF00400 | 0.585 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.429 |
DOC_CYCLIN_RxL_1 | 362 | 372 | PF00134 | 0.517 |
DOC_CYCLIN_yCln2_LP_2 | 239 | 245 | PF00134 | 0.383 |
DOC_CYCLIN_yCln2_LP_2 | 57 | 63 | PF00134 | 0.445 |
DOC_MAPK_DCC_7 | 96 | 104 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 72 | 79 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 96 | 104 | PF00069 | 0.427 |
DOC_PP1_RVXF_1 | 365 | 371 | PF00149 | 0.517 |
DOC_PP2B_LxvP_1 | 283 | 286 | PF13499 | 0.546 |
DOC_PP2B_LxvP_1 | 38 | 41 | PF13499 | 0.485 |
DOC_PP2B_LxvP_1 | 57 | 60 | PF13499 | 0.450 |
DOC_PP4_FxxP_1 | 97 | 100 | PF00568 | 0.382 |
DOC_SPAK_OSR1_1 | 96 | 100 | PF12202 | 0.383 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.413 |
DOC_USP7_UBL2_3 | 17 | 21 | PF12436 | 0.598 |
DOC_USP7_UBL2_3 | 313 | 317 | PF12436 | 0.447 |
DOC_USP7_UBL2_3 | 42 | 46 | PF12436 | 0.600 |
DOC_USP7_UBL2_3 | 486 | 490 | PF12436 | 0.541 |
DOC_USP7_UBL2_3 | 498 | 502 | PF12436 | 0.482 |
DOC_USP7_UBL2_3 | 509 | 513 | PF12436 | 0.568 |
DOC_USP7_UBL2_3 | 515 | 519 | PF12436 | 0.549 |
DOC_USP7_UBL2_3 | 521 | 525 | PF12436 | 0.526 |
LIG_14-3-3_CanoR_1 | 193 | 203 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 244 | 254 | PF00244 | 0.345 |
LIG_BRCT_BRCA1_1 | 93 | 97 | PF00533 | 0.388 |
LIG_CSL_BTD_1 | 1 | 4 | PF09270 | 0.426 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.577 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.480 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.480 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.450 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.446 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.409 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.599 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.454 |
LIG_LIR_Apic_2 | 94 | 100 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 165 | 174 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 183 | 189 | PF02991 | 0.209 |
LIG_LIR_Gen_1 | 247 | 258 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 356 | 365 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 165 | 169 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.227 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.442 |
LIG_MYND_1 | 294 | 298 | PF01753 | 0.519 |
LIG_PCNA_PIPBox_1 | 337 | 346 | PF02747 | 0.392 |
LIG_PTB_Apo_2 | 352 | 359 | PF02174 | 0.517 |
LIG_PTB_Apo_2 | 45 | 52 | PF02174 | 0.539 |
LIG_PTB_Phospho_1 | 45 | 51 | PF10480 | 0.540 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.318 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.319 |
LIG_SH2_CRK | 321 | 325 | PF00017 | 0.466 |
LIG_SH2_CRK | 328 | 332 | PF00017 | 0.447 |
LIG_SH2_PTP2 | 234 | 237 | PF00017 | 0.311 |
LIG_SH2_SRC | 51 | 54 | PF00017 | 0.473 |
LIG_SH2_STAT3 | 127 | 130 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.173 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.569 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.545 |
LIG_SUMO_SIM_anti_2 | 31 | 39 | PF11976 | 0.297 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.559 |
LIG_TRAF2_1 | 409 | 412 | PF00917 | 0.517 |
LIG_TYR_ITSM | 246 | 253 | PF00017 | 0.428 |
LIG_UBA3_1 | 37 | 42 | PF00899 | 0.465 |
LIG_UBA3_1 | 416 | 425 | PF00899 | 0.440 |
LIG_WRC_WIRS_1 | 163 | 168 | PF05994 | 0.469 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.326 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.520 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.658 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.434 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.483 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.440 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.365 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.506 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.371 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.385 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.499 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.513 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.337 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.465 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.424 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.387 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.237 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.260 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.346 |
MOD_GlcNHglycan | 467 | 471 | PF01048 | 0.705 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.466 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.412 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.442 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.427 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.347 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.457 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.502 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.423 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.388 |
MOD_N-GLC_1 | 476 | 481 | PF02516 | 0.457 |
MOD_N-GLC_2 | 101 | 103 | PF02516 | 0.448 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.527 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.459 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.428 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.325 |
MOD_PIKK_1 | 272 | 278 | PF00454 | 0.399 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.446 |
MOD_PK_1 | 30 | 36 | PF00069 | 0.312 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.381 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.383 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.464 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.412 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.313 |
MOD_Plk_2-3 | 432 | 438 | PF00069 | 0.753 |
MOD_Plk_2-3 | 448 | 454 | PF00069 | 0.660 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.320 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.465 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.420 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.428 |
MOD_SUMO_for_1 | 16 | 19 | PF00179 | 0.594 |
MOD_SUMO_for_1 | 20 | 23 | PF00179 | 0.588 |
MOD_SUMO_for_1 | 409 | 412 | PF00179 | 0.517 |
MOD_SUMO_rev_2 | 136 | 145 | PF00179 | 0.476 |
MOD_SUMO_rev_2 | 14 | 22 | PF00179 | 0.585 |
TRG_DiLeu_BaEn_1 | 292 | 297 | PF01217 | 0.418 |
TRG_DiLeu_BaEn_1 | 412 | 417 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.440 |
TRG_ER_diArg_1 | 243 | 246 | PF00400 | 0.366 |
TRG_NLS_Bipartite_1 | 509 | 528 | PF00514 | 0.443 |
TRG_NLS_MonoCore_2 | 479 | 484 | PF00514 | 0.682 |
TRG_NLS_MonoExtC_3 | 479 | 484 | PF00514 | 0.563 |
TRG_NLS_MonoExtC_3 | 523 | 529 | PF00514 | 0.455 |
TRG_NLS_MonoExtN_4 | 521 | 528 | PF00514 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 367 | 372 | PF00026 | 0.280 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PG07 | Leptomonas seymouri | 79% | 100% |
A0A0S4IUW8 | Bodo saltans | 31% | 100% |
A0A1X0P6K5 | Trypanosomatidae | 40% | 91% |
A0A3Q8IGI0 | Leishmania donovani | 87% | 100% |
A0A422P127 | Trypanosoma rangeli | 45% | 95% |
A4I7I5 | Leishmania infantum | 87% | 100% |
D0A088 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 96% |
E9B2E2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
O01683 | Caenorhabditis elegans | 24% | 77% |
O94529 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 100% |
P41848 | Caenorhabditis elegans | 24% | 76% |
Q04636 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 97% |
Q04678 | Gallus gallus | 23% | 75% |
Q04931 | Rattus norvegicus | 22% | 75% |
Q05153 | Arabidopsis thaliana | 20% | 83% |
Q05344 | Drosophila melanogaster | 24% | 74% |
Q08943 | Mus musculus | 22% | 75% |
Q08945 | Homo sapiens | 23% | 75% |
Q293F6 | Drosophila pseudoobscura pseudoobscura | 24% | 73% |
Q2USL9 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 23% | 93% |
Q39601 | Catharanthus roseus | 24% | 83% |
Q4IJU0 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 21% | 94% |
Q4Q5R4 | Leishmania major | 87% | 100% |
Q4WGK6 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 23% | 93% |
Q5ALL8 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 25% | 99% |
Q5AYE3 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 23% | 93% |
Q6CWD7 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 24% | 96% |
Q6FKI2 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 25% | 98% |
Q756X6 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 98% |
Q7RWW0 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 21% | 94% |
Q9LEF5 | Zea mays | 23% | 83% |
Q9LGR0 | Oryza sativa subsp. japonica | 22% | 83% |
Q9W602 | Xenopus laevis | 22% | 77% |