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: 1 |
NetGPI | no | yes: 0, no: 1 |
Related structures:
AlphaFold database: E9AHX9
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 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:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 2 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 2 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 509 | 511 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 552 | 554 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.443 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 552 | 554 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 588 | 590 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.414 |
DEG_SPOP_SBC_1 | 469 | 473 | PF00917 | 0.489 |
DEG_SPOP_SBC_1 | 476 | 480 | PF00917 | 0.486 |
DOC_CDC14_PxL_1 | 535 | 543 | PF14671 | 0.271 |
DOC_CKS1_1 | 318 | 323 | PF01111 | 0.445 |
DOC_CYCLIN_RxL_1 | 157 | 167 | PF00134 | 0.228 |
DOC_CYCLIN_RxL_1 | 357 | 364 | PF00134 | 0.266 |
DOC_MAPK_gen_1 | 51 | 60 | PF00069 | 0.278 |
DOC_MAPK_MEF2A_6 | 210 | 217 | PF00069 | 0.233 |
DOC_MAPK_MEF2A_6 | 231 | 239 | PF00069 | 0.254 |
DOC_MAPK_MEF2A_6 | 536 | 543 | PF00069 | 0.270 |
DOC_PIKK_1 | 201 | 208 | PF02985 | 0.241 |
DOC_PP2B_LxvP_1 | 290 | 293 | PF13499 | 0.442 |
DOC_PP2B_LxvP_1 | 80 | 83 | PF13499 | 0.249 |
DOC_PP4_FxxP_1 | 318 | 321 | PF00568 | 0.447 |
DOC_PP4_FxxP_1 | 407 | 410 | PF00568 | 0.266 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.279 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.276 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.371 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.287 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.273 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.245 |
LIG_14-3-3_CanoR_1 | 289 | 293 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 504 | 512 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 552 | 560 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 561 | 566 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 59 | 67 | PF00244 | 0.271 |
LIG_14-3-3_CterR_2 | 614 | 619 | PF00244 | 0.450 |
LIG_Actin_WH2_2 | 374 | 392 | PF00022 | 0.279 |
LIG_BRCT_BRCA1_1 | 170 | 174 | PF00533 | 0.279 |
LIG_Clathr_ClatBox_1 | 236 | 240 | PF01394 | 0.278 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.241 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.488 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.365 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.446 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.274 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.244 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.483 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.323 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.313 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.291 |
LIG_FHA_2 | 444 | 450 | PF00498 | 0.472 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.486 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.416 |
LIG_LIR_Apic_2 | 315 | 321 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 194 | 205 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 277 | 284 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 542 | 551 | PF02991 | 0.321 |
LIG_LIR_LC3C_4 | 196 | 200 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 117 | 121 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 277 | 282 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 542 | 546 | PF02991 | 0.283 |
LIG_MYND_3 | 538 | 542 | PF01753 | 0.271 |
LIG_NRBOX | 540 | 546 | PF00104 | 0.276 |
LIG_Pex14_1 | 572 | 576 | PF04695 | 0.420 |
LIG_Pex14_2 | 568 | 572 | PF04695 | 0.401 |
LIG_PTB_Apo_2 | 401 | 408 | PF02174 | 0.276 |
LIG_SH2_NCK_1 | 20 | 24 | PF00017 | 0.322 |
LIG_SH2_PTP2 | 81 | 84 | PF00017 | 0.232 |
LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.237 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.240 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.232 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.268 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.303 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.412 |
LIG_Sin3_3 | 161 | 168 | PF02671 | 0.229 |
LIG_SUMO_SIM_anti_2 | 5 | 11 | PF11976 | 0.265 |
LIG_SUMO_SIM_anti_2 | 542 | 548 | PF11976 | 0.291 |
LIG_SUMO_SIM_par_1 | 234 | 240 | PF11976 | 0.274 |
LIG_SUMO_SIM_par_1 | 424 | 430 | PF11976 | 0.278 |
LIG_TRAF2_1 | 68 | 71 | PF00917 | 0.306 |
LIG_UBA3_1 | 605 | 612 | PF00899 | 0.436 |
LIG_WRC_WIRS_1 | 276 | 281 | PF05994 | 0.244 |
MOD_CDC14_SPxK_1 | 32 | 35 | PF00782 | 0.404 |
MOD_CDK_SPxK_1 | 29 | 35 | PF00069 | 0.413 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.460 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.261 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.246 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.253 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.484 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.490 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.486 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.268 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.276 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.427 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.333 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.317 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.278 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.470 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.484 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.298 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.275 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.387 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.442 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.485 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.435 |
MOD_GlcNHglycan | 458 | 462 | PF01048 | 0.501 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.492 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.490 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.481 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.306 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.452 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.371 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.498 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.483 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.415 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.255 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.368 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.470 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.498 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.486 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.409 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.267 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.247 |
MOD_N-GLC_1 | 465 | 470 | PF02516 | 0.497 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.430 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.411 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.245 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.322 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.253 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.275 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.256 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.431 |
MOD_NEK2_2 | 352 | 357 | PF00069 | 0.273 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.276 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.427 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.434 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.485 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.358 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.472 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.280 |
MOD_Plk_1 | 523 | 529 | PF00069 | 0.384 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.464 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.242 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.253 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.280 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.278 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.265 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.413 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.485 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.491 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.448 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.245 |
TRG_DiLeu_BaEn_1 | 56 | 61 | PF01217 | 0.263 |
TRG_DiLeu_BaLyEn_6 | 533 | 538 | PF01217 | 0.301 |
TRG_DiLeu_BaLyEn_6 | 80 | 85 | PF01217 | 0.239 |
TRG_DiLeu_LyEn_5 | 56 | 61 | PF01217 | 0.263 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.240 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.232 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.292 |
TRG_ER_diArg_1 | 588 | 590 | PF00400 | 0.404 |
TRG_NES_CRM1_1 | 206 | 221 | PF08389 | 0.234 |
TRG_Pf-PMV_PEXEL_1 | 245 | 250 | PF00026 | 0.227 |