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: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 23 |
GO:0042995 | cell projection | 2 | 23 |
GO:0043226 | organelle | 2 | 23 |
GO:0043227 | membrane-bounded organelle | 3 | 23 |
GO:0110165 | cellular anatomical entity | 1 | 23 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 23 |
GO:0005743 | mitochondrial inner membrane | 5 | 1 |
GO:0016020 | membrane | 2 | 1 |
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 | 2 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 2 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: E9AIU4
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009987 | cellular process | 1 | 4 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0010498 | proteasomal protein catabolic process | 5 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006457 | protein folding | 2 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007021 | tubulin complex assembly | 6 | 1 |
GO:0007023 | post-chaperonin tubulin folding pathway | 3 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
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 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0043014 | alpha-tubulin binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 198 | 202 | PF00656 | 0.419 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.454 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.341 |
CLV_PCSK_PC1ET2_1 | 294 | 296 | PF00082 | 0.292 |
CLV_PCSK_PC7_1 | 290 | 296 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.363 |
DEG_APCC_DBOX_1 | 18 | 26 | PF00400 | 0.317 |
DEG_SCF_FBW7_1 | 401 | 408 | PF00400 | 0.253 |
DOC_CDC14_PxL_1 | 254 | 262 | PF14671 | 0.299 |
DOC_CDC14_PxL_1 | 72 | 80 | PF14671 | 0.350 |
DOC_CYCLIN_RxL_1 | 165 | 174 | PF00134 | 0.450 |
DOC_CYCLIN_RxL_1 | 256 | 268 | PF00134 | 0.464 |
DOC_CYCLIN_RxL_1 | 95 | 106 | PF00134 | 0.421 |
DOC_MAPK_MEF2A_6 | 256 | 264 | PF00069 | 0.300 |
DOC_MAPK_MEF2A_6 | 484 | 493 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 510 | 518 | PF00069 | 0.277 |
DOC_MAPK_RevD_3 | 279 | 295 | PF00069 | 0.272 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.223 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.291 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.436 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.522 |
LIG_14-3-3_CanoR_1 | 117 | 122 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 188 | 194 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 19 | 28 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 223 | 230 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 234 | 240 | PF00244 | 0.369 |
LIG_Actin_WH2_2 | 257 | 275 | PF00022 | 0.241 |
LIG_Clathr_ClatBox_1 | 479 | 483 | PF01394 | 0.429 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.387 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.360 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.343 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.352 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.531 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.457 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.475 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.444 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.228 |
LIG_LIR_Gen_1 | 120 | 129 | PF02991 | 0.222 |
LIG_LIR_Gen_1 | 145 | 156 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 285 | 296 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 448 | 455 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 483 | 493 | PF02991 | 0.233 |
LIG_LIR_Gen_1 | 494 | 502 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 520 | 529 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 120 | 124 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 448 | 452 | PF02991 | 0.199 |
LIG_LIR_Nem_3 | 483 | 489 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 492 | 498 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 520 | 526 | PF02991 | 0.310 |
LIG_MYND_3 | 75 | 79 | PF01753 | 0.225 |
LIG_NRBOX | 259 | 265 | PF00104 | 0.267 |
LIG_SH2_CRK | 495 | 499 | PF00017 | 0.292 |
LIG_SH2_GRB2like | 148 | 151 | PF00017 | 0.253 |
LIG_SH2_NCK_1 | 495 | 499 | PF00017 | 0.245 |
LIG_SH2_NCK_1 | 523 | 527 | PF00017 | 0.296 |
LIG_SH2_SRC | 523 | 526 | PF00017 | 0.298 |
LIG_SH2_STAP1 | 523 | 527 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.305 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.466 |
LIG_SUMO_SIM_anti_2 | 417 | 423 | PF11976 | 0.228 |
LIG_SUMO_SIM_par_1 | 191 | 198 | PF11976 | 0.338 |
LIG_TRAF2_1 | 351 | 354 | PF00917 | 0.278 |
LIG_TYR_ITIM | 146 | 151 | PF00017 | 0.260 |
LIG_TYR_ITIM | 493 | 498 | PF00017 | 0.447 |
LIG_UBA3_1 | 146 | 153 | PF00899 | 0.439 |
LIG_UBA3_1 | 330 | 337 | PF00899 | 0.320 |
LIG_UBA3_1 | 511 | 517 | PF00899 | 0.271 |
LIG_WRC_WIRS_1 | 118 | 123 | PF05994 | 0.238 |
LIG_WRC_WIRS_1 | 421 | 426 | PF05994 | 0.207 |
LIG_WRC_WIRS_1 | 446 | 451 | PF05994 | 0.213 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.403 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.518 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.351 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.466 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.307 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.475 |
MOD_CK2_1 | 459 | 465 | PF00069 | 0.285 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.310 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.290 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.508 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.288 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.391 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.335 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.396 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.483 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.377 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.305 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.399 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.439 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.390 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.393 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.370 |
MOD_N-GLC_1 | 215 | 220 | PF02516 | 0.428 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.469 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.357 |
MOD_N-GLC_1 | 540 | 545 | PF02516 | 0.369 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.308 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.390 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.331 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.378 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.337 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.427 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.536 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.295 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.466 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.448 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.378 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.384 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.440 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.355 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.325 |
MOD_NEK2_2 | 380 | 385 | PF00069 | 0.536 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.287 |
MOD_PIKK_1 | 540 | 546 | PF00454 | 0.326 |
MOD_PKA_1 | 503 | 509 | PF00069 | 0.235 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.424 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.464 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.425 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.405 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.417 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.377 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.241 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.565 |
MOD_Plk_2-3 | 348 | 354 | PF00069 | 0.378 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.519 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.321 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.525 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.381 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.404 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.394 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.413 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.417 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.528 |
MOD_SUMO_rev_2 | 280 | 289 | PF00179 | 0.305 |
MOD_SUMO_rev_2 | 408 | 418 | PF00179 | 0.333 |
TRG_AP2beta_CARGO_1 | 285 | 295 | PF09066 | 0.280 |
TRG_DiLeu_BaLyEn_6 | 258 | 263 | PF01217 | 0.372 |
TRG_DiLeu_BaLyEn_6 | 270 | 275 | PF01217 | 0.229 |
TRG_DiLeu_BaLyEn_6 | 326 | 331 | PF01217 | 0.322 |
TRG_DiLeu_BaLyEn_6 | 364 | 369 | PF01217 | 0.270 |
TRG_DiLeu_BaLyEn_6 | 507 | 512 | PF01217 | 0.325 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 495 | 498 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 523 | 526 | PF00928 | 0.301 |
TRG_ER_diArg_1 | 396 | 398 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 502 | 504 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 85 | 88 | PF00400 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 350 | 354 | PF00026 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2F4 | Leptomonas seymouri | 27% | 100% |
A0A0N1P921 | Leptomonas seymouri | 24% | 68% |
A0A0S4JR64 | Bodo saltans | 24% | 85% |
A0A1X0NG16 | Trypanosomatidae | 25% | 95% |
A0A1X0P4M6 | Trypanosomatidae | 25% | 95% |
A0A3Q8IGD6 | Leishmania donovani | 77% | 68% |
A0A3S5H7C2 | Leishmania donovani | 25% | 100% |
A0A3S5ISR4 | Trypanosoma rangeli | 28% | 66% |
A4HCY0 | Leishmania braziliensis | 25% | 100% |
A4I0G3 | Leishmania infantum | 25% | 100% |
A4I6T8 | Leishmania infantum | 77% | 68% |
C9ZRQ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AEF0 | Leishmania major | 24% | 71% |
E9AWC6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B1W0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 68% |
Q4Q6A2 | Leishmania major | 76% | 100% |
Q4QB46 | Leishmania major | 25% | 100% |
Q4QD45 | Leishmania major | 26% | 82% |
Q4QJ80 | Leishmania major | 26% | 97% |
V5BKI3 | Trypanosoma cruzi | 26% | 66% |
V5BMQ2 | Trypanosoma cruzi | 24% | 99% |