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: 1, no: 23 |
NetGPI | no | yes: 0, no: 24 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 25 |
GO:0042995 | cell projection | 2 | 25 |
GO:0043226 | organelle | 2 | 25 |
GO:0043227 | membrane-bounded organelle | 3 | 25 |
GO:0110165 | cellular anatomical entity | 1 | 25 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 25 |
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: A4H4H0
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 4 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 4 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016310 | phosphorylation | 5 | 4 |
GO:0044237 | cellular metabolic process | 2 | 5 |
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 | 4 |
GO:0016301 | kinase activity | 4 | 4 |
GO:0016740 | transferase activity | 2 | 4 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 267 | 271 | PF00656 | 0.294 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.445 |
CLV_PCSK_FUR_1 | 89 | 93 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.443 |
CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.217 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.491 |
DEG_SCF_FBW7_1 | 56 | 62 | PF00400 | 0.510 |
DOC_CDC14_PxL_1 | 206 | 214 | PF14671 | 0.518 |
DOC_CDC14_PxL_1 | 325 | 333 | PF14671 | 0.453 |
DOC_CKS1_1 | 178 | 183 | PF01111 | 0.280 |
DOC_CKS1_1 | 56 | 61 | PF01111 | 0.715 |
DOC_CYCLIN_RxL_1 | 1 | 12 | PF00134 | 0.460 |
DOC_CYCLIN_RxL_1 | 199 | 208 | PF00134 | 0.547 |
DOC_CYCLIN_RxL_1 | 279 | 291 | PF00134 | 0.430 |
DOC_CYCLIN_RxL_1 | 352 | 362 | PF00134 | 0.245 |
DOC_CYCLIN_RxL_1 | 374 | 385 | PF00134 | 0.293 |
DOC_MAPK_gen_1 | 188 | 195 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 521 | 531 | PF00069 | 0.539 |
DOC_PP1_RVXF_1 | 102 | 109 | PF00149 | 0.510 |
DOC_PP4_FxxP_1 | 17 | 20 | PF00568 | 0.651 |
DOC_PP4_FxxP_1 | 43 | 46 | PF00568 | 0.461 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.285 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.431 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.298 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.724 |
LIG_14-3-3_CanoR_1 | 235 | 240 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 279 | 287 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 316 | 325 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 380 | 389 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 435 | 443 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 444 | 450 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 524 | 531 | PF00244 | 0.371 |
LIG_Actin_WH2_2 | 344 | 362 | PF00022 | 0.287 |
LIG_Actin_WH2_2 | 412 | 429 | PF00022 | 0.365 |
LIG_APCC_ABBAyCdc20_2 | 91 | 97 | PF00400 | 0.365 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.515 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.497 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.470 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.386 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.454 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.457 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.616 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.337 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.170 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.664 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.391 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.501 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.363 |
LIG_LIR_Apic_2 | 96 | 102 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 308 | 317 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 197 | 201 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 308 | 312 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 343 | 348 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.605 |
LIG_MLH1_MIPbox_1 | 104 | 108 | PF16413 | 0.328 |
LIG_MYND_3 | 209 | 213 | PF01753 | 0.298 |
LIG_MYND_3 | 328 | 332 | PF01753 | 0.547 |
LIG_PDZ_Class_1 | 530 | 535 | PF00595 | 0.600 |
LIG_PTB_Apo_2 | 303 | 310 | PF02174 | 0.213 |
LIG_PTB_Phospho_1 | 303 | 309 | PF10480 | 0.217 |
LIG_SH2_SRC | 309 | 312 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.427 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.315 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.688 |
LIG_SUMO_SIM_anti_2 | 117 | 122 | PF11976 | 0.527 |
LIG_SUMO_SIM_anti_2 | 129 | 135 | PF11976 | 0.465 |
LIG_SUMO_SIM_anti_2 | 299 | 305 | PF11976 | 0.525 |
LIG_SUMO_SIM_anti_2 | 69 | 77 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 223 | 232 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 237 | 242 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 299 | 305 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 355 | 362 | PF11976 | 0.448 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.285 |
LIG_TRAF2_1 | 517 | 520 | PF00917 | 0.350 |
LIG_TYR_ITIM | 307 | 312 | PF00017 | 0.263 |
LIG_TYR_ITIM | 496 | 501 | PF00017 | 0.454 |
LIG_WRC_WIRS_1 | 342 | 347 | PF05994 | 0.225 |
MOD_CDK_SPxK_1 | 438 | 444 | PF00069 | 0.346 |
MOD_CDK_SPxxK_3 | 28 | 35 | PF00069 | 0.474 |
MOD_CDK_SPxxK_3 | 438 | 445 | PF00069 | 0.241 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.511 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.459 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.424 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.530 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.510 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.595 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.362 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.486 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.556 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.691 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.650 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.362 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.585 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.582 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.415 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.410 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.597 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.331 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.467 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.414 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.368 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.569 |
MOD_N-GLC_1 | 164 | 169 | PF02516 | 0.475 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.304 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.379 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.478 |
MOD_N-GLC_1 | 508 | 513 | PF02516 | 0.555 |
MOD_N-GLC_2 | 290 | 292 | PF02516 | 0.413 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.642 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.405 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.410 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.520 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.427 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.363 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.343 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.630 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.329 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.368 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.213 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.326 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.393 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.386 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.584 |
MOD_NEK2_2 | 102 | 107 | PF00069 | 0.504 |
MOD_NEK2_2 | 229 | 234 | PF00069 | 0.307 |
MOD_OFUCOSY | 408 | 415 | PF10250 | 0.291 |
MOD_PIKK_1 | 279 | 285 | PF00454 | 0.357 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.619 |
MOD_PKA_1 | 444 | 450 | PF00069 | 0.459 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.439 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.367 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.555 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.355 |
MOD_PKB_1 | 314 | 322 | PF00069 | 0.229 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.577 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.472 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.403 |
MOD_Plk_1 | 513 | 519 | PF00069 | 0.428 |
MOD_Plk_2-3 | 514 | 520 | PF00069 | 0.481 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.434 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.465 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.459 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.330 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.446 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.696 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.292 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.698 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.425 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.475 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.391 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.502 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.304 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.431 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.725 |
TRG_DiLeu_BaLyEn_6 | 89 | 94 | PF01217 | 0.350 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.265 |
TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.448 |
TRG_ER_diArg_1 | 314 | 317 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 88 | 91 | PF00400 | 0.544 |
TRG_NES_CRM1_1 | 350 | 361 | PF08389 | 0.392 |
TRG_NLS_MonoExtC_3 | 187 | 192 | PF00514 | 0.294 |
TRG_Pf-PMV_PEXEL_1 | 326 | 330 | PF00026 | 0.347 |
TRG_Pf-PMV_PEXEL_1 | 4 | 9 | PF00026 | 0.642 |
TRG_Pf-PMV_PEXEL_1 | 91 | 96 | PF00026 | 0.601 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8N9 | Leptomonas seymouri | 25% | 81% |
A0A0N1IHY9 | Leptomonas seymouri | 56% | 100% |
A0A0S4IJS8 | Bodo saltans | 27% | 100% |
A0A0S4IK76 | Bodo saltans | 26% | 98% |
A0A0S4IRN7 | Bodo saltans | 26% | 100% |
A0A0S4KN43 | Bodo saltans | 27% | 91% |
A0A3S5H5M6 | Leishmania donovani | 87% | 100% |
A0A3S7X2V4 | Leishmania donovani | 25% | 69% |
A0A3S7X7D2 | Leishmania donovani | 26% | 100% |
A4H7G0 | Leishmania braziliensis | 23% | 100% |
A4HSP5 | Leishmania infantum | 87% | 100% |
A4I9H0 | Leishmania infantum | 26% | 100% |
C9ZRQ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
C9ZUA8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 72% |
C9ZXN7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZZI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 88% |
D0A0X4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 79% |
E9AEF0 | Leishmania major | 24% | 69% |
E9AHJ6 | Leishmania infantum | 25% | 69% |
E9AKN0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
E9APJ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
P23799 | Trypanosoma brucei brucei | 25% | 85% |
P26337 | Trypanosoma equiperdum | 23% | 85% |
Q4QJ77 | Leishmania major | 85% | 100% |
V5BMQ2 | Trypanosoma cruzi | 23% | 95% |