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:0005634 | nucleus | 5 | 10 |
GO:0005840 | ribosome | 5 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043228 | non-membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:1990904 | ribonucleoprotein complex | 2 | 7 |
GO:0000417 | HIR complex | 2 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4ICF6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006325 | chromatin organization | 4 | 11 |
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 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
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 | 11 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 174 | 178 | PF00656 | 0.550 |
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.426 |
CLV_C14_Caspase3-7 | 80 | 84 | PF00656 | 0.489 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.744 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.597 |
CLV_PCSK_FUR_1 | 467 | 471 | PF00082 | 0.518 |
CLV_PCSK_FUR_1 | 616 | 620 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.618 |
CLV_PCSK_PC1ET2_1 | 371 | 373 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 618 | 620 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.136 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.219 |
CLV_Separin_Fungi | 573 | 579 | PF03568 | 0.471 |
DEG_SPOP_SBC_1 | 446 | 450 | PF00917 | 0.729 |
DOC_CYCLIN_yClb1_LxF_4 | 331 | 337 | PF00134 | 0.372 |
DOC_MAPK_gen_1 | 116 | 124 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 566 | 574 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 566 | 574 | PF00069 | 0.476 |
DOC_PP1_RVXF_1 | 241 | 248 | PF00149 | 0.283 |
DOC_PP1_RVXF_1 | 299 | 306 | PF00149 | 0.405 |
DOC_PP1_RVXF_1 | 417 | 424 | PF00149 | 0.293 |
DOC_PP2B_LxvP_1 | 312 | 315 | PF13499 | 0.364 |
DOC_PP2B_LxvP_1 | 422 | 425 | PF13499 | 0.329 |
DOC_PP4_FxxP_1 | 427 | 430 | PF00568 | 0.369 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.336 |
DOC_USP7_MATH_1 | 629 | 633 | PF00917 | 0.576 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.344 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 551 | 556 | PF00397 | 0.527 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 252 | 258 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 413 | 422 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 500 | 507 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 510 | 517 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 569 | 575 | PF00244 | 0.444 |
LIG_AP2alpha_2 | 248 | 250 | PF02296 | 0.320 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.544 |
LIG_deltaCOP1_diTrp_1 | 248 | 257 | PF00928 | 0.323 |
LIG_deltaCOP1_diTrp_1 | 40 | 45 | PF00928 | 0.477 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.513 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.448 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.564 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.355 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.285 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.426 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.513 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.603 |
LIG_FHA_2 | 622 | 628 | PF00498 | 0.575 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.485 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.433 |
LIG_LIR_Gen_1 | 248 | 257 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 502 | 512 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 530 | 538 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 119 | 124 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 502 | 507 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 530 | 535 | PF02991 | 0.286 |
LIG_NRBOX | 559 | 565 | PF00104 | 0.519 |
LIG_PDZ_Class_1 | 646 | 651 | PF00595 | 0.562 |
LIG_Pex14_1 | 423 | 427 | PF04695 | 0.324 |
LIG_Pex14_2 | 253 | 257 | PF04695 | 0.411 |
LIG_SH2_CRK | 300 | 304 | PF00017 | 0.372 |
LIG_SH2_CRK | 316 | 320 | PF00017 | 0.432 |
LIG_SH2_PTP2 | 532 | 535 | PF00017 | 0.284 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 525 | 529 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.403 |
LIG_SH3_2 | 30 | 35 | PF14604 | 0.422 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.480 |
LIG_SH3_3 | 625 | 631 | PF00018 | 0.645 |
LIG_SUMO_SIM_anti_2 | 38 | 43 | PF11976 | 0.345 |
LIG_SUMO_SIM_anti_2 | 610 | 616 | PF11976 | 0.664 |
LIG_TRAF2_1 | 7 | 10 | PF00917 | 0.519 |
LIG_TYR_ITIM | 298 | 303 | PF00017 | 0.452 |
LIG_TYR_ITIM | 314 | 319 | PF00017 | 0.235 |
LIG_UBA3_1 | 333 | 342 | PF00899 | 0.553 |
LIG_WRC_WIRS_1 | 254 | 259 | PF05994 | 0.304 |
MOD_CDK_SPxxK_3 | 551 | 558 | PF00069 | 0.528 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.702 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.370 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.275 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.453 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.604 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.675 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.387 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.441 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.612 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.604 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.589 |
MOD_CMANNOS | 247 | 250 | PF00535 | 0.309 |
MOD_Cter_Amidation | 368 | 371 | PF01082 | 0.512 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.283 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.486 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.572 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.580 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.312 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.388 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.377 |
MOD_GlcNHglycan | 365 | 369 | PF01048 | 0.619 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.469 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.608 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.702 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.415 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.707 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.529 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.388 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.414 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.611 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.610 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.725 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.474 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.371 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.571 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.435 |
MOD_LATS_1 | 508 | 514 | PF00433 | 0.359 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.467 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.199 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.521 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.376 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.369 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.345 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.284 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.547 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.454 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.449 |
MOD_NEK2_2 | 343 | 348 | PF00069 | 0.390 |
MOD_PIKK_1 | 438 | 444 | PF00454 | 0.574 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.533 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.436 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.436 |
MOD_PKA_2 | 499 | 505 | PF00069 | 0.373 |
MOD_PKA_2 | 577 | 583 | PF00069 | 0.567 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.497 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.547 |
MOD_Plk_1 | 519 | 525 | PF00069 | 0.407 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.417 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.256 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.394 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.550 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.342 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.328 |
MOD_ProDKin_1 | 551 | 557 | PF00069 | 0.526 |
MOD_SUMO_for_1 | 270 | 273 | PF00179 | 0.548 |
MOD_SUMO_for_1 | 7 | 10 | PF00179 | 0.519 |
MOD_SUMO_rev_2 | 137 | 144 | PF00179 | 0.319 |
MOD_SUMO_rev_2 | 178 | 187 | PF00179 | 0.538 |
TRG_DiLeu_BaEn_1 | 50 | 55 | PF01217 | 0.549 |
TRG_DiLeu_BaEn_4 | 50 | 56 | PF01217 | 0.463 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.284 |
TRG_ER_diArg_1 | 277 | 279 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 34 | 37 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 467 | 470 | PF00400 | 0.565 |
TRG_NLS_MonoCore_2 | 615 | 620 | PF00514 | 0.556 |
TRG_NLS_MonoExtC_3 | 615 | 620 | PF00514 | 0.556 |
TRG_NLS_MonoExtN_4 | 616 | 621 | PF00514 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 510 | 514 | PF00026 | 0.329 |
TRG_PTS2 | 1 | 45 | PF00400 | 0.530 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBV3 | Leptomonas seymouri | 62% | 95% |
A0A1X0P8Z1 | Trypanosomatidae | 47% | 100% |
A0A3S7XAX4 | Leishmania donovani | 100% | 100% |
A0A422NCI3 | Trypanosoma rangeli | 48% | 100% |
A4HPB6 | Leishmania braziliensis | 78% | 100% |
D0A3C6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AT27 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
O13985 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 100% |
Q4Q1H1 | Leishmania major | 90% | 100% |
V5BH36 | Trypanosoma cruzi | 48% | 100% |