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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9B423
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 12 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 12 |
GO:0042254 | ribosome biogenesis | 5 | 11 |
GO:0044085 | cellular component biogenesis | 3 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0042273 | ribosomal large subunit biogenesis | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0003924 | GTPase activity | 7 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 435 | 439 | PF00656 | 0.232 |
CLV_C14_Caspase3-7 | 536 | 540 | PF00656 | 0.693 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.232 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.232 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.583 |
CLV_PCSK_FUR_1 | 394 | 398 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 131 | 133 | PF00082 | 0.232 |
CLV_PCSK_PC1ET2_1 | 525 | 527 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 548 | 550 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.103 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 490 | 494 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 605 | 609 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.225 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.232 |
CLV_Separin_Metazoa | 391 | 395 | PF03568 | 0.616 |
DEG_APCC_DBOX_1 | 131 | 139 | PF00400 | 0.232 |
DOC_CKS1_1 | 221 | 226 | PF01111 | 0.279 |
DOC_CYCLIN_RxL_1 | 201 | 211 | PF00134 | 0.300 |
DOC_CYCLIN_yCln2_LP_2 | 373 | 379 | PF00134 | 0.418 |
DOC_MAPK_gen_1 | 188 | 196 | PF00069 | 0.326 |
DOC_MAPK_gen_1 | 490 | 498 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 547 | 555 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 17 | 24 | PF00069 | 0.232 |
DOC_PIKK_1 | 460 | 468 | PF02985 | 0.537 |
DOC_PP1_RVXF_1 | 48 | 55 | PF00149 | 0.247 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.641 |
DOC_USP7_UBL2_3 | 26 | 30 | PF12436 | 0.247 |
DOC_USP7_UBL2_3 | 493 | 497 | PF12436 | 0.431 |
DOC_USP7_UBL2_3 | 53 | 57 | PF12436 | 0.232 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.273 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.232 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.526 |
LIG_14-3-3_CanoR_1 | 137 | 145 | PF00244 | 0.232 |
LIG_14-3-3_CanoR_1 | 396 | 405 | PF00244 | 0.245 |
LIG_14-3-3_CanoR_1 | 418 | 422 | PF00244 | 0.268 |
LIG_14-3-3_CanoR_1 | 511 | 520 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 549 | 554 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 587 | 592 | PF00244 | 0.502 |
LIG_Actin_WH2_2 | 103 | 121 | PF00022 | 0.232 |
LIG_Actin_WH2_2 | 321 | 336 | PF00022 | 0.455 |
LIG_Clathr_ClatBox_1 | 253 | 257 | PF01394 | 0.232 |
LIG_Clathr_ClatBox_1 | 454 | 458 | PF01394 | 0.377 |
LIG_DLG_GKlike_1 | 549 | 557 | PF00625 | 0.552 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.281 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.314 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.317 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.232 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.232 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.541 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.247 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.461 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.212 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.268 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.321 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.313 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.331 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.232 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.232 |
LIG_Integrin_RGD_1 | 593 | 595 | PF01839 | 0.613 |
LIG_LIR_Gen_1 | 113 | 120 | PF02991 | 0.232 |
LIG_LIR_Gen_1 | 18 | 24 | PF02991 | 0.233 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 352 | 363 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.232 |
LIG_LIR_Nem_3 | 15 | 19 | PF02991 | 0.230 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 271 | 276 | PF02991 | 0.232 |
LIG_LIR_Nem_3 | 352 | 358 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 595 | 600 | PF02991 | 0.451 |
LIG_MYND_1 | 631 | 635 | PF01753 | 0.435 |
LIG_NRP_CendR_1 | 649 | 652 | PF00754 | 0.470 |
LIG_PTB_Apo_2 | 357 | 364 | PF02174 | 0.377 |
LIG_PTB_Phospho_1 | 357 | 363 | PF10480 | 0.377 |
LIG_Rb_pABgroove_1 | 82 | 90 | PF01858 | 0.232 |
LIG_SH2_CRK | 355 | 359 | PF00017 | 0.448 |
LIG_SH2_GRB2like | 443 | 446 | PF00017 | 0.247 |
LIG_SH2_NCK_1 | 443 | 447 | PF00017 | 0.232 |
LIG_SH2_PTP2 | 114 | 117 | PF00017 | 0.232 |
LIG_SH2_SRC | 443 | 446 | PF00017 | 0.244 |
LIG_SH2_STAT3 | 65 | 68 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.232 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.330 |
LIG_SUMO_SIM_anti_2 | 9 | 15 | PF11976 | 0.254 |
LIG_SUMO_SIM_par_1 | 170 | 175 | PF11976 | 0.277 |
LIG_SUMO_SIM_par_1 | 453 | 458 | PF11976 | 0.395 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.398 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.368 |
LIG_TRAF2_1 | 311 | 314 | PF00917 | 0.356 |
LIG_TRAF2_1 | 459 | 462 | PF00917 | 0.473 |
LIG_WW_3 | 391 | 395 | PF00397 | 0.616 |
MOD_CDK_SPxxK_3 | 363 | 370 | PF00069 | 0.530 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.322 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.527 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.603 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.550 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.378 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.344 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.248 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.259 |
MOD_GlcNHglycan | 257 | 261 | PF01048 | 0.326 |
MOD_GlcNHglycan | 350 | 354 | PF01048 | 0.401 |
MOD_GlcNHglycan | 539 | 543 | PF01048 | 0.607 |
MOD_GlcNHglycan | 563 | 567 | PF01048 | 0.570 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.547 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.232 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.288 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.245 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.232 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.622 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.546 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.563 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.529 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.227 |
MOD_N-GLC_2 | 290 | 292 | PF02516 | 0.330 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.270 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.238 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.237 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.232 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.468 |
MOD_NEK2_2 | 120 | 125 | PF00069 | 0.232 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.232 |
MOD_PIKK_1 | 512 | 518 | PF00454 | 0.543 |
MOD_PIKK_1 | 52 | 58 | PF00454 | 0.232 |
MOD_PIKK_1 | 526 | 532 | PF00454 | 0.429 |
MOD_PK_1 | 161 | 167 | PF00069 | 0.232 |
MOD_PK_1 | 533 | 539 | PF00069 | 0.681 |
MOD_PK_1 | 551 | 557 | PF00069 | 0.553 |
MOD_PK_1 | 587 | 593 | PF00069 | 0.534 |
MOD_PKA_1 | 396 | 402 | PF00069 | 0.272 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.554 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.246 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.272 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.499 |
MOD_PKB_1 | 394 | 402 | PF00069 | 0.266 |
MOD_PKB_1 | 547 | 555 | PF00069 | 0.546 |
MOD_PKB_1 | 562 | 570 | PF00069 | 0.513 |
MOD_PKB_1 | 585 | 593 | PF00069 | 0.520 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.378 |
MOD_Plk_1 | 585 | 591 | PF00069 | 0.541 |
MOD_Plk_2-3 | 293 | 299 | PF00069 | 0.317 |
MOD_Plk_2-3 | 417 | 423 | PF00069 | 0.232 |
MOD_Plk_2-3 | 477 | 483 | PF00069 | 0.510 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.232 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.297 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.305 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.273 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.232 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.438 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.375 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.276 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.232 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.426 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.528 |
MOD_SUMO_for_1 | 499 | 502 | PF00179 | 0.442 |
MOD_SUMO_rev_2 | 327 | 336 | PF00179 | 0.258 |
TRG_DiLeu_BaEn_2 | 373 | 379 | PF01217 | 0.484 |
TRG_DiLeu_BaEn_2 | 486 | 492 | PF01217 | 0.397 |
TRG_DiLeu_BaEn_4 | 460 | 466 | PF01217 | 0.388 |
TRG_DiLeu_BaLyEn_6 | 113 | 118 | PF01217 | 0.232 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.232 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.247 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.232 |
TRG_ENDOCYTIC_2 | 597 | 600 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.246 |
TRG_ER_diArg_1 | 393 | 396 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 510 | 512 | PF00400 | 0.493 |
TRG_NLS_MonoExtC_3 | 546 | 551 | PF00514 | 0.587 |
TRG_NLS_MonoExtN_4 | 545 | 552 | PF00514 | 0.620 |
TRG_Pf-PMV_PEXEL_1 | 615 | 620 | PF00026 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE10 | Leptomonas seymouri | 93% | 100% |
A0A0S4IM98 | Bodo saltans | 79% | 100% |
A0A1X0P3L0 | Trypanosomatidae | 84% | 100% |
A0A3S5IQL0 | Trypanosoma rangeli | 81% | 100% |
A0A3S7X6S7 | Leishmania donovani | 98% | 100% |
A4HLP8 | Leishmania braziliensis | 95% | 100% |
A4I949 | Leishmania infantum | 97% | 100% |
D0A6C6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 81% | 100% |
G0S8F1 | Chaetomium thermophilum (strain DSM 1495 / CBS 144.50 / IMI 039719) | 44% | 99% |
O44411 | Caenorhabditis elegans | 44% | 96% |
O94659 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 47% | 100% |
Q02892 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 43% | 100% |
Q4Q401 | Leishmania major | 98% | 100% |
Q54N72 | Dictyostelium discoideum | 47% | 97% |
Q6CM00 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 42% | 100% |
Q6FRV0 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 42% | 100% |
Q74ZK6 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 44% | 100% |
Q8SVJ8 | Encephalitozoon cuniculi (strain GB-M1) | 50% | 100% |
Q99ME9 | Mus musculus | 50% | 100% |
Q99P77 | Rattus norvegicus | 48% | 100% |
Q9BZE4 | Homo sapiens | 50% | 100% |
Q9C6I8 | Arabidopsis thaliana | 50% | 97% |
Q9U6A9 | Trypanosoma brucei brucei | 81% | 100% |
Q9V411 | Drosophila melanogaster | 48% | 100% |
V5BYN7 | Trypanosoma cruzi | 82% | 100% |