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:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HPI5
Term | Name | Level | Count |
---|---|---|---|
GO:0006417 | regulation of translation | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0010628 | positive regulation of gene expression | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0034248 | regulation of amide metabolic process | 5 | 1 |
GO:0034250 | positive regulation of amide metabolic process | 6 | 1 |
GO:0045727 | positive regulation of translation | 7 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 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:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051247 | positive regulation of protein metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 1 |
GO:2000765 | regulation of cytoplasmic translation | 7 | 1 |
GO:2000767 | positive regulation of cytoplasmic translation | 8 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008270 | zinc ion binding | 6 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003727 | single-stranded RNA binding | 5 | 1 |
GO:0003729 | mRNA binding | 5 | 1 |
GO:0045182 | translation regulator activity | 1 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004540 | RNA nuclease activity | 4 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 368 | 372 | PF00656 | 0.279 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 509 | 511 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.217 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 336 | 338 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 424 | 426 | PF00082 | 0.443 |
CLV_PCSK_PC1ET2_1 | 449 | 451 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 74 | 76 | PF00082 | 0.368 |
CLV_PCSK_PC1ET2_1 | 89 | 91 | PF00082 | 0.424 |
CLV_PCSK_PC7_1 | 58 | 64 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.459 |
DOC_CKS1_1 | 39 | 44 | PF01111 | 0.452 |
DOC_CYCLIN_RxL_1 | 543 | 553 | PF00134 | 0.471 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 69 | 76 | PF00134 | 0.335 |
DOC_MAPK_gen_1 | 336 | 345 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 483 | 491 | PF00069 | 0.384 |
DOC_MAPK_MEF2A_6 | 336 | 345 | PF00069 | 0.398 |
DOC_PP1_RVXF_1 | 557 | 564 | PF00149 | 0.483 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.478 |
DOC_PP2B_LxvP_1 | 332 | 335 | PF13499 | 0.411 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.495 |
DOC_USP7_MATH_2 | 283 | 289 | PF00917 | 0.545 |
DOC_USP7_UBL2_3 | 532 | 536 | PF12436 | 0.466 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 109 | 113 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 181 | 187 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 278 | 283 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 357 | 363 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 452 | 459 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 551 | 561 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 90 | 98 | PF00244 | 0.737 |
LIG_14-3-3_CterR_2 | 570 | 573 | PF00244 | 0.393 |
LIG_APCC_ABBA_1 | 477 | 482 | PF00400 | 0.476 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.498 |
LIG_Clathr_ClatBox_1 | 16 | 20 | PF01394 | 0.645 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.531 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.429 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.355 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.311 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.345 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.597 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.435 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.383 |
LIG_GBD_Chelix_1 | 440 | 448 | PF00786 | 0.393 |
LIG_LIR_Gen_1 | 397 | 408 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 497 | 502 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 560 | 566 | PF02991 | 0.575 |
LIG_LYPXL_S_1 | 498 | 502 | PF13949 | 0.337 |
LIG_LYPXL_yS_3 | 499 | 502 | PF13949 | 0.343 |
LIG_MYND_1 | 14 | 18 | PF01753 | 0.642 |
LIG_PDZ_Class_1 | 568 | 573 | PF00595 | 0.358 |
LIG_SH2_CRK | 265 | 269 | PF00017 | 0.695 |
LIG_SH2_PTP2 | 329 | 332 | PF00017 | 0.526 |
LIG_SH2_SRC | 366 | 369 | PF00017 | 0.302 |
LIG_SH2_STAP1 | 375 | 379 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.651 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.236 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.389 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.483 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.608 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.488 |
LIG_SUMO_SIM_anti_2 | 338 | 346 | PF11976 | 0.275 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.647 |
LIG_TYR_ITIM | 128 | 133 | PF00017 | 0.485 |
LIG_WRC_WIRS_1 | 563 | 568 | PF05994 | 0.320 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.490 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.613 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.670 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.539 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.695 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.518 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.522 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.467 |
MOD_CK2_1 | 550 | 556 | PF00069 | 0.459 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.528 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.599 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.491 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.550 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.525 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.574 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.392 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.382 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.266 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.673 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.542 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.545 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.708 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.482 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.314 |
MOD_LATS_1 | 235 | 241 | PF00433 | 0.434 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.633 |
MOD_N-GLC_1 | 358 | 363 | PF02516 | 0.517 |
MOD_N-GLC_2 | 232 | 234 | PF02516 | 0.427 |
MOD_N-GLC_2 | 71 | 73 | PF02516 | 0.396 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.499 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.358 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.343 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.527 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.363 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.486 |
MOD_NEK2_2 | 504 | 509 | PF00069 | 0.440 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.364 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.628 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.502 |
MOD_PKA_1 | 509 | 515 | PF00069 | 0.567 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.582 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.387 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.729 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.323 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.355 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.429 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.541 |
MOD_PKB_1 | 423 | 431 | PF00069 | 0.555 |
MOD_PKB_1 | 450 | 458 | PF00069 | 0.599 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.557 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.365 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.467 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.514 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.436 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.504 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.589 |
TRG_DiLeu_BaLyEn_6 | 543 | 548 | PF01217 | 0.496 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.431 |
TRG_ER_diArg_1 | 356 | 358 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 422 | 425 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 508 | 510 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 61 | 63 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.223 |
TRG_NLS_Bipartite_1 | 74 | 93 | PF00514 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 425 | 429 | PF00026 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 546 | 550 | PF00026 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIN4 | Leptomonas seymouri | 72% | 100% |
A0A1X0P496 | Trypanosomatidae | 52% | 100% |
A0A3Q8IKH2 | Leishmania donovani | 86% | 100% |
A0A3R7MHM2 | Trypanosoma rangeli | 52% | 100% |
A4IDA7 | Leishmania infantum | 86% | 100% |
D0A8E8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9AT97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q1A0 | Leishmania major | 85% | 100% |
V5DA56 | Trypanosoma cruzi | 52% | 100% |