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:0032991 | protein-containing complex | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
GO:0005840 | ribosome | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HJ40
Term | Name | Level | Count |
---|---|---|---|
GO:0001514 | selenocysteine incorporation | 7 | 1 |
GO:0006414 | translational elongation | 5 | 1 |
GO:0006417 | regulation of translation | 6 | 1 |
GO:0006451 | translational readthrough | 6 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0034248 | regulation of amide metabolic process | 5 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003729 | mRNA binding | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0035368 | selenocysteine insertion sequence binding | 6 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003730 | mRNA 3'-UTR binding | 6 | 1 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 253 | 257 | PF00656 | 0.716 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.534 |
CLV_PCSK_FUR_1 | 212 | 216 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 203 | 205 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 24 | 26 | PF00082 | 0.658 |
CLV_PCSK_PC1ET2_1 | 98 | 100 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.403 |
DEG_APCC_DBOX_1 | 105 | 113 | PF00400 | 0.399 |
DEG_APCC_DBOX_1 | 409 | 417 | PF00400 | 0.391 |
DEG_APCC_DBOX_1 | 534 | 542 | PF00400 | 0.398 |
DEG_SPOP_SBC_1 | 36 | 40 | PF00917 | 0.584 |
DEG_SPOP_SBC_1 | 447 | 451 | PF00917 | 0.440 |
DOC_CKS1_1 | 112 | 117 | PF01111 | 0.441 |
DOC_CKS1_1 | 84 | 89 | PF01111 | 0.505 |
DOC_CYCLIN_yCln2_LP_2 | 318 | 324 | PF00134 | 0.374 |
DOC_MAPK_gen_1 | 105 | 111 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 203 | 213 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 382 | 389 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 390 | 399 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 404 | 413 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 519 | 528 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 93 | 103 | PF00069 | 0.490 |
DOC_MAPK_MEF2A_6 | 407 | 415 | PF00069 | 0.465 |
DOC_PP2B_LxvP_1 | 430 | 433 | PF13499 | 0.465 |
DOC_PP4_FxxP_1 | 266 | 269 | PF00568 | 0.550 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.517 |
DOC_USP7_MATH_2 | 14 | 20 | PF00917 | 0.504 |
DOC_USP7_UBL2_3 | 24 | 28 | PF12436 | 0.762 |
DOC_USP7_UBL2_3 | 457 | 461 | PF12436 | 0.632 |
DOC_USP7_UBL2_3 | 73 | 77 | PF12436 | 0.484 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.624 |
LIG_14-3-3_CanoR_1 | 175 | 181 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 220 | 226 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 509 | 515 | PF00244 | 0.535 |
LIG_BRCT_BRCA1_1 | 346 | 350 | PF00533 | 0.489 |
LIG_CaM_IQ_9 | 396 | 412 | PF13499 | 0.469 |
LIG_EVH1_1 | 430 | 434 | PF00568 | 0.463 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.536 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.310 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.516 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.588 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.409 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.399 |
LIG_FHA_2 | 552 | 558 | PF00498 | 0.464 |
LIG_Integrin_RGD_1 | 227 | 229 | PF01839 | 0.370 |
LIG_LIR_Apic_2 | 265 | 269 | PF02991 | 0.558 |
LIG_LIR_Apic_2 | 442 | 448 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 182 | 191 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 365 | 375 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 261 | 266 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 320 | 325 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.337 |
LIG_LYPXL_yS_3 | 291 | 294 | PF13949 | 0.464 |
LIG_NRBOX | 221 | 227 | PF00104 | 0.357 |
LIG_PCNA_yPIPBox_3 | 301 | 315 | PF02747 | 0.381 |
LIG_Pex14_1 | 107 | 111 | PF04695 | 0.390 |
LIG_SH2_CRK | 322 | 326 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 514 | 518 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 544 | 548 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 552 | 556 | PF00017 | 0.361 |
LIG_SH2_STAT3 | 375 | 378 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.473 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.569 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.636 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.466 |
LIG_SUMO_SIM_par_1 | 412 | 419 | PF11976 | 0.412 |
LIG_TRFH_1 | 46 | 50 | PF08558 | 0.480 |
LIG_UBA3_1 | 370 | 376 | PF00899 | 0.452 |
LIG_WRC_WIRS_1 | 263 | 268 | PF05994 | 0.632 |
MOD_CDC14_SPxK_1 | 261 | 264 | PF00782 | 0.441 |
MOD_CDK_SPxK_1 | 258 | 264 | PF00069 | 0.448 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.628 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.418 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.442 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.614 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.608 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.591 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.555 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.564 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.417 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.724 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.352 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.414 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.455 |
MOD_Cter_Amidation | 75 | 78 | PF01082 | 0.508 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.499 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.426 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.636 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.693 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.689 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.589 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.551 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.674 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.425 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.628 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.596 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.782 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.671 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.568 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.357 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.699 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.385 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.558 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.630 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.626 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.477 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.367 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.481 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.495 |
MOD_NEK2_2 | 262 | 267 | PF00069 | 0.451 |
MOD_NEK2_2 | 463 | 468 | PF00069 | 0.514 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.551 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.592 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.542 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.711 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.421 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.402 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.641 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.438 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.679 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.534 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.645 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.549 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.556 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.393 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.430 |
MOD_Plk_1 | 556 | 562 | PF00069 | 0.448 |
MOD_Plk_2-3 | 314 | 320 | PF00069 | 0.511 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.431 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.357 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.521 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.538 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.437 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.626 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.532 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.659 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.620 |
TRG_DiLeu_BaEn_1 | 469 | 474 | PF01217 | 0.405 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.470 |
TRG_ER_diArg_1 | 105 | 107 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 25 | 27 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 392 | 395 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 410 | 413 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 509 | 512 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 91 | 94 | PF00400 | 0.622 |
TRG_NLS_MonoCore_2 | 22 | 27 | PF00514 | 0.515 |
TRG_NLS_MonoExtC_3 | 22 | 27 | PF00514 | 0.515 |
TRG_NLS_MonoExtC_3 | 381 | 386 | PF00514 | 0.422 |
TRG_NLS_MonoExtN_4 | 23 | 28 | PF00514 | 0.511 |
TRG_NLS_MonoExtN_4 | 457 | 464 | PF00514 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 546 | 550 | PF00026 | 0.260 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMN8 | Leptomonas seymouri | 50% | 100% |
A0A1X0NJ63 | Trypanosomatidae | 30% | 89% |
A0A3R7LBH7 | Trypanosoma rangeli | 31% | 100% |
A0A3S7X464 | Leishmania donovani | 68% | 100% |
A4I6F5 | Leishmania infantum | 69% | 100% |
C9ZN70 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B1L2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
Q9BHF1 | Leishmania major | 70% | 99% |
V5BDV6 | Trypanosoma cruzi | 29% | 95% |