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:0005634 | nucleus | 5 | 11 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0000417 | HIR complex | 2 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005840 | ribosome | 5 | 6 |
GO:0032991 | protein-containing complex | 1 | 6 |
GO:0043228 | non-membrane-bounded organelle | 3 | 6 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 6 |
GO:1990904 | ribonucleoprotein complex | 2 | 6 |
Related structures:
AlphaFold database: A4HPB6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006325 | chromatin organization | 4 | 12 |
GO:0006351 | DNA-templated transcription | 7 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009059 | macromolecule biosynthetic process | 4 | 11 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0018130 | heterocycle biosynthetic process | 4 | 11 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 11 |
GO:0032774 | RNA biosynthetic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:0097659 | nucleic acid-templated transcription | 6 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
GO:0006335 | DNA replication-dependent chromatin assembly | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 162 | 166 | PF00656 | 0.517 |
CLV_C14_Caspase3-7 | 631 | 635 | PF00656 | 0.505 |
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.488 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 598 | 600 | PF00675 | 0.782 |
CLV_NRD_NRD_1 | 622 | 624 | PF00675 | 0.620 |
CLV_PCSK_FUR_1 | 476 | 480 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 598 | 600 | PF00082 | 0.712 |
CLV_PCSK_PC7_1 | 425 | 431 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.155 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.237 |
DEG_SPOP_SBC_1 | 443 | 447 | PF00917 | 0.529 |
DEG_SPOP_SBC_1 | 614 | 618 | PF00917 | 0.671 |
DOC_MAPK_gen_1 | 104 | 112 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 20 | 29 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 575 | 583 | PF00069 | 0.560 |
DOC_PP1_RVXF_1 | 227 | 234 | PF00149 | 0.324 |
DOC_PP1_RVXF_1 | 285 | 292 | PF00149 | 0.413 |
DOC_PP1_RVXF_1 | 403 | 410 | PF00149 | 0.321 |
DOC_PP2B_LxvP_1 | 298 | 301 | PF13499 | 0.405 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.361 |
DOC_PP4_FxxP_1 | 413 | 416 | PF00568 | 0.481 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 615 | 619 | PF00917 | 0.715 |
DOC_USP7_UBL2_3 | 626 | 630 | PF12436 | 0.502 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 560 | 565 | PF00397 | 0.617 |
LIG_14-3-3_CanoR_1 | 104 | 110 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 238 | 244 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 399 | 408 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 509 | 516 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 519 | 526 | PF00244 | 0.342 |
LIG_AP2alpha_2 | 234 | 236 | PF02296 | 0.341 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.634 |
LIG_deltaCOP1_diTrp_1 | 234 | 243 | PF00928 | 0.338 |
LIG_deltaCOP1_diTrp_1 | 28 | 33 | PF00928 | 0.529 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.539 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.367 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.461 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.391 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.650 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.616 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.470 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.328 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.563 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.655 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.691 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.507 |
LIG_FHA_2 | 601 | 607 | PF00498 | 0.577 |
LIG_FHA_2 | 629 | 635 | PF00498 | 0.718 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.448 |
LIG_Integrin_RGD_1 | 604 | 606 | PF01839 | 0.524 |
LIG_LIR_Gen_1 | 234 | 243 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 511 | 521 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 539 | 547 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 285 | 289 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 511 | 516 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 539 | 544 | PF02991 | 0.320 |
LIG_NRBOX | 568 | 574 | PF00104 | 0.586 |
LIG_PDZ_Class_1 | 652 | 657 | PF00595 | 0.640 |
LIG_Pex14_1 | 409 | 413 | PF04695 | 0.383 |
LIG_Pex14_2 | 239 | 243 | PF04695 | 0.440 |
LIG_SH2_CRK | 286 | 290 | PF00017 | 0.407 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.514 |
LIG_SH2_CRK | 359 | 363 | PF00017 | 0.498 |
LIG_SH2_PTP2 | 541 | 544 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 185 | 189 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 384 | 388 | PF00017 | 0.305 |
LIG_SH2_STAP1 | 534 | 538 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.319 |
LIG_SUMO_SIM_anti_2 | 26 | 31 | PF11976 | 0.398 |
LIG_SUMO_SIM_anti_2 | 616 | 623 | PF11976 | 0.714 |
LIG_TYR_ITIM | 284 | 289 | PF00017 | 0.489 |
LIG_TYR_ITIM | 300 | 305 | PF00017 | 0.298 |
LIG_UBA3_1 | 319 | 328 | PF00899 | 0.630 |
LIG_WRC_WIRS_1 | 240 | 245 | PF05994 | 0.338 |
LIG_WRC_WIRS_1 | 557 | 562 | PF05994 | 0.423 |
MOD_CDK_SPxxK_3 | 560 | 567 | PF00069 | 0.610 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.726 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.404 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.448 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.557 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.488 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.410 |
MOD_CK1_1 | 559 | 565 | PF00069 | 0.511 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.538 |
MOD_CMANNOS | 233 | 236 | PF00535 | 0.330 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.442 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.302 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.485 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.604 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.280 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.339 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.690 |
MOD_GlcNHglycan | 606 | 610 | PF01048 | 0.664 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.450 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.534 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.539 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.543 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.458 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.761 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.549 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.546 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.615 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.501 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.427 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.474 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.560 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.636 |
MOD_LATS_1 | 517 | 523 | PF00433 | 0.401 |
MOD_N-GLC_1 | 47 | 52 | PF02516 | 0.347 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.503 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.216 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.410 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.378 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.309 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.495 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.458 |
MOD_PIKK_1 | 464 | 470 | PF00454 | 0.557 |
MOD_PKA_1 | 598 | 604 | PF00069 | 0.710 |
MOD_PKA_1 | 625 | 631 | PF00069 | 0.594 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.479 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.499 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.396 |
MOD_PKA_2 | 586 | 592 | PF00069 | 0.634 |
MOD_PKA_2 | 598 | 604 | PF00069 | 0.687 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.561 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.438 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.443 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.461 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.437 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.399 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.357 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.476 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.355 |
MOD_ProDKin_1 | 560 | 566 | PF00069 | 0.610 |
MOD_SUMO_rev_2 | 125 | 132 | PF00179 | 0.355 |
MOD_SUMO_rev_2 | 164 | 173 | PF00179 | 0.567 |
TRG_DiLeu_BaEn_1 | 38 | 43 | PF01217 | 0.576 |
TRG_DiLeu_BaEn_4 | 38 | 44 | PF01217 | 0.494 |
TRG_DiLeu_BaLyEn_6 | 461 | 466 | PF01217 | 0.434 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.331 |
TRG_ER_diArg_1 | 22 | 25 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 263 | 265 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.320 |
TRG_ER_diArg_1 | 476 | 479 | PF00400 | 0.615 |
TRG_NES_CRM1_1 | 372 | 387 | PF08389 | 0.342 |
TRG_NLS_MonoCore_2 | 622 | 627 | PF00514 | 0.571 |
TRG_NLS_MonoExtC_3 | 622 | 627 | PF00514 | 0.571 |
TRG_NLS_MonoExtN_4 | 623 | 628 | PF00514 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 519 | 523 | PF00026 | 0.367 |
TRG_PTS2 | 1 | 33 | PF00400 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBV3 | Leptomonas seymouri | 63% | 96% |
A0A0S4JTR4 | Bodo saltans | 31% | 100% |
A0A1X0P8Z1 | Trypanosomatidae | 46% | 100% |
A0A3S7XAX4 | Leishmania donovani | 78% | 100% |
A0A422NCI3 | Trypanosoma rangeli | 49% | 100% |
A4ICF6 | Leishmania infantum | 78% | 100% |
D0A3C6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AT27 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 97% |
Q4Q1H1 | Leishmania major | 81% | 100% |
V5BH36 | Trypanosoma cruzi | 47% | 100% |