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: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 21 |
GO:0042995 | cell projection | 2 | 21 |
GO:0043226 | organelle | 2 | 21 |
GO:0043227 | membrane-bounded organelle | 3 | 21 |
GO:0110165 | cellular anatomical entity | 1 | 21 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 21 |
GO:0005743 | mitochondrial inner membrane | 5 | 1 |
GO:0016020 | membrane | 2 | 2 |
GO:0019866 | organelle inner membrane | 4 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031966 | mitochondrial membrane | 4 | 1 |
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: Q4QJ77
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016310 | phosphorylation | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016301 | kinase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 267 | 271 | PF00656 | 0.498 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.471 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.494 |
DEG_SCF_FBW7_1 | 56 | 62 | PF00400 | 0.521 |
DOC_CDC14_PxL_1 | 206 | 214 | PF14671 | 0.428 |
DOC_CDC14_PxL_1 | 325 | 333 | PF14671 | 0.312 |
DOC_CKS1_1 | 344 | 349 | PF01111 | 0.294 |
DOC_CKS1_1 | 56 | 61 | PF01111 | 0.714 |
DOC_CYCLIN_RxL_1 | 199 | 208 | PF00134 | 0.531 |
DOC_MAPK_gen_1 | 188 | 195 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 521 | 531 | PF00069 | 0.602 |
DOC_MAPK_MEF2A_6 | 374 | 383 | PF00069 | 0.294 |
DOC_PP1_RVXF_1 | 102 | 109 | PF00149 | 0.572 |
DOC_PP4_FxxP_1 | 43 | 46 | PF00568 | 0.516 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.309 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.437 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.733 |
LIG_14-3-3_CanoR_1 | 235 | 240 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 258 | 264 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 294 | 301 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 380 | 389 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 397 | 401 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 435 | 443 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 524 | 531 | PF00244 | 0.567 |
LIG_Actin_WH2_2 | 67 | 83 | PF00022 | 0.449 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.505 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.576 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.619 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.532 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.417 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.340 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.452 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.719 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.550 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.341 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.418 |
LIG_FHA_2 | 507 | 513 | PF00498 | 0.476 |
LIG_LIR_Apic_2 | 97 | 102 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 306 | 317 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 197 | 201 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 343 | 348 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.640 |
LIG_MLH1_MIPbox_1 | 104 | 108 | PF16413 | 0.425 |
LIG_MYND_3 | 209 | 213 | PF01753 | 0.351 |
LIG_MYND_3 | 328 | 332 | PF01753 | 0.305 |
LIG_PDZ_Class_1 | 530 | 535 | PF00595 | 0.637 |
LIG_PTB_Apo_2 | 93 | 100 | PF02174 | 0.409 |
LIG_PTB_Phospho_1 | 93 | 99 | PF10480 | 0.409 |
LIG_SH2_SRC | 309 | 312 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.353 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.719 |
LIG_SUMO_SIM_anti_2 | 117 | 122 | PF11976 | 0.543 |
LIG_SUMO_SIM_anti_2 | 299 | 306 | PF11976 | 0.324 |
LIG_SUMO_SIM_anti_2 | 69 | 77 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 237 | 242 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 340 | 346 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 355 | 362 | PF11976 | 0.355 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.339 |
LIG_TRAF2_1 | 517 | 520 | PF00917 | 0.417 |
LIG_TYR_ITIM | 307 | 312 | PF00017 | 0.311 |
LIG_TYR_ITIM | 496 | 501 | PF00017 | 0.432 |
LIG_WRC_WIRS_1 | 247 | 252 | PF05994 | 0.470 |
MOD_CDK_SPxxK_3 | 28 | 35 | PF00069 | 0.605 |
MOD_CDK_SPxxK_3 | 390 | 397 | PF00069 | 0.482 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.564 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.666 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.357 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.472 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.395 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.521 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.622 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.527 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.409 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.477 |
MOD_CK2_1 | 506 | 512 | PF00069 | 0.525 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.458 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.601 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.658 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.686 |
MOD_GlcNHglycan | 216 | 220 | PF01048 | 0.448 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.380 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.337 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.524 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.387 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.348 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.398 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.479 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.515 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.626 |
MOD_N-GLC_1 | 164 | 169 | PF02516 | 0.513 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.421 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.433 |
MOD_N-GLC_2 | 290 | 292 | PF02516 | 0.459 |
MOD_N-GLC_2 | 432 | 434 | PF02516 | 0.398 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.504 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.658 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.546 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.549 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.658 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.519 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.362 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.318 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.644 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.372 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.388 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.361 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.341 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.557 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.631 |
MOD_NEK2_2 | 102 | 107 | PF00069 | 0.538 |
MOD_NEK2_2 | 229 | 234 | PF00069 | 0.352 |
MOD_NEK2_2 | 350 | 355 | PF00069 | 0.543 |
MOD_NEK2_2 | 422 | 427 | PF00069 | 0.471 |
MOD_OFUCOSY | 408 | 415 | PF10250 | 0.358 |
MOD_PIKK_1 | 177 | 183 | PF00454 | 0.560 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.501 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.681 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.504 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.511 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.384 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.451 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.503 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.312 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.580 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.552 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.459 |
MOD_Plk_2-3 | 514 | 520 | PF00069 | 0.538 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.531 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.369 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.387 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.521 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.519 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.608 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.407 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.503 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.414 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.445 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.459 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.364 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.730 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.436 |
TRG_ER_diArg_1 | 314 | 317 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 88 | 91 | PF00400 | 0.655 |
TRG_NLS_MonoExtC_3 | 187 | 192 | PF00514 | 0.345 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8N9 | Leptomonas seymouri | 25% | 81% |
A0A0N1IHY9 | Leptomonas seymouri | 57% | 100% |
A0A0S4ITQ8 | Bodo saltans | 24% | 100% |
A0A0S4J578 | Bodo saltans | 28% | 71% |
A0A1X0P4M6 | Trypanosomatidae | 24% | 92% |
A0A3S5H5M6 | Leishmania donovani | 97% | 100% |
A0A3S7X2V4 | Leishmania donovani | 28% | 69% |
A4H3R1 | Leishmania braziliensis | 23% | 77% |
A4H4H0 | Leishmania braziliensis | 85% | 100% |
A4HSP5 | Leishmania infantum | 97% | 100% |
C9ZRQ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
C9ZS86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 99% |
C9ZUA8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 72% |
C9ZZI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 88% |
D0A0X4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 79% |
E9AEF0 | Leishmania major | 26% | 69% |
E9AHJ6 | Leishmania infantum | 28% | 69% |
E9AKN0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
P26337 | Trypanosoma equiperdum | 25% | 85% |
V5BMQ2 | Trypanosoma cruzi | 26% | 95% |