Protein modification, ubiquitin hydrolase
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: 10 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4I7U2
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 12 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 10 |
GO:0009057 | macromolecule catabolic process | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016579 | protein deubiquitination | 6 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 10 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 10 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 10 |
GO:0070646 | protein modification by small protein removal | 5 | 12 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901575 | organic substance catabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004843 | cysteine-type deubiquitinase activity | 5 | 12 |
GO:0008233 | peptidase activity | 3 | 12 |
GO:0008234 | cysteine-type peptidase activity | 4 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 12 |
GO:0101005 | deubiquitinase activity | 5 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.334 |
CLV_PCSK_FUR_1 | 430 | 434 | PF00082 | 0.286 |
CLV_PCSK_FUR_1 | 98 | 102 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.366 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.425 |
DEG_SPOP_SBC_1 | 269 | 273 | PF00917 | 0.303 |
DOC_CYCLIN_RxL_1 | 430 | 440 | PF00134 | 0.339 |
DOC_MAPK_DCC_7 | 399 | 408 | PF00069 | 0.320 |
DOC_MAPK_gen_1 | 308 | 315 | PF00069 | 0.339 |
DOC_MAPK_gen_1 | 343 | 352 | PF00069 | 0.327 |
DOC_MAPK_gen_1 | 392 | 400 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 430 | 437 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 345 | 354 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 356 | 364 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 399 | 408 | PF00069 | 0.320 |
DOC_MAPK_RevD_3 | 398 | 413 | PF00069 | 0.390 |
DOC_PP2B_LxvP_1 | 265 | 268 | PF13499 | 0.245 |
DOC_PP2B_LxvP_1 | 435 | 438 | PF13499 | 0.304 |
DOC_PP4_FxxP_1 | 58 | 61 | PF00568 | 0.571 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.346 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.391 |
DOC_USP7_UBL2_3 | 308 | 312 | PF12436 | 0.362 |
DOC_USP7_UBL2_3 | 392 | 396 | PF12436 | 0.309 |
DOC_USP7_UBL2_3 | 524 | 528 | PF12436 | 0.425 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.601 |
LIG_14-3-3_CanoR_1 | 107 | 112 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 349 | 353 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 378 | 386 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 430 | 436 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 455 | 460 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 81 | 87 | PF00244 | 0.585 |
LIG_BRCT_BRCA1_1 | 404 | 408 | PF00533 | 0.450 |
LIG_Clathr_ClatBox_1 | 242 | 246 | PF01394 | 0.425 |
LIG_Clathr_ClatBox_1 | 422 | 426 | PF01394 | 0.339 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.400 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.364 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.314 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.281 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.342 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.329 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.404 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.402 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.389 |
LIG_Integrin_RGD_1 | 463 | 465 | PF01839 | 0.425 |
LIG_LIR_Apic_2 | 173 | 179 | PF02991 | 0.354 |
LIG_LIR_Apic_2 | 355 | 361 | PF02991 | 0.425 |
LIG_LIR_Apic_2 | 56 | 61 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 114 | 121 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 128 | 137 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 145 | 153 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 405 | 416 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 75 | 82 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 114 | 118 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 145 | 149 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 405 | 411 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 529 | 535 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.301 |
LIG_MYND_1 | 189 | 193 | PF01753 | 0.451 |
LIG_NRBOX | 230 | 236 | PF00104 | 0.362 |
LIG_Pex14_1 | 172 | 176 | PF04695 | 0.320 |
LIG_Pex14_1 | 177 | 181 | PF04695 | 0.320 |
LIG_Pex14_2 | 142 | 146 | PF04695 | 0.339 |
LIG_PTB_Apo_2 | 124 | 131 | PF02174 | 0.238 |
LIG_Rb_pABgroove_1 | 71 | 79 | PF01858 | 0.328 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.451 |
LIG_SH2_CRK | 454 | 458 | PF00017 | 0.339 |
LIG_SH2_CRK | 77 | 81 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.487 |
LIG_SH3_2 | 57 | 62 | PF14604 | 0.468 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.623 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.451 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.617 |
LIG_SUMO_SIM_anti_2 | 348 | 355 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 149 | 154 | PF11976 | 0.443 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.339 |
LIG_TYR_ITSM | 528 | 535 | PF00017 | 0.425 |
LIG_WRC_WIRS_1 | 143 | 148 | PF05994 | 0.409 |
LIG_WW_3 | 59 | 63 | PF00397 | 0.573 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.420 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.325 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.389 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.382 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.406 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.412 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.431 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.710 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.608 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.417 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.329 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.455 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.588 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.350 |
MOD_LATS_1 | 300 | 306 | PF00433 | 0.245 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.274 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.413 |
MOD_N-GLC_1 | 516 | 521 | PF02516 | 0.429 |
MOD_N-GLC_2 | 129 | 131 | PF02516 | 0.320 |
MOD_N-GLC_2 | 42 | 44 | PF02516 | 0.543 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.490 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.355 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.319 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.121 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.331 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.387 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.305 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.661 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.320 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.586 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.378 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.678 |
MOD_PK_1 | 402 | 408 | PF00069 | 0.245 |
MOD_PK_1 | 455 | 461 | PF00069 | 0.451 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.451 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.522 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.320 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.194 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.299 |
MOD_Plk_1 | 516 | 522 | PF00069 | 0.425 |
MOD_Plk_2-3 | 256 | 262 | PF00069 | 0.440 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.417 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.374 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.398 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.308 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.364 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.363 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.336 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.390 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.425 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.391 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.430 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.602 |
MOD_SUMO_rev_2 | 387 | 394 | PF00179 | 0.245 |
TRG_DiLeu_BaEn_2 | 528 | 534 | PF01217 | 0.390 |
TRG_DiLeu_BaEn_4 | 240 | 246 | PF01217 | 0.451 |
TRG_DiLeu_BaLyEn_6 | 452 | 457 | PF01217 | 0.425 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.318 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.351 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.708 |
TRG_Pf-PMV_PEXEL_1 | 74 | 78 | PF00026 | 0.318 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMP3 | Leptomonas seymouri | 57% | 100% |
A0A0S4IXL6 | Bodo saltans | 33% | 99% |
A0A1X0NUI1 | Trypanosomatidae | 45% | 100% |
A0A3S7X5G6 | Leishmania donovani | 98% | 100% |
A0A422P1B8 | Trypanosoma rangeli | 43% | 100% |
A4HKB2 | Leishmania braziliensis | 78% | 99% |
A5PJS6 | Bos taurus | 24% | 68% |
D0AA02 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B2Q0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 98% |
P52479 | Mus musculus | 25% | 68% |
Q14694 | Homo sapiens | 24% | 68% |
Q2NL57 | Xenopus laevis | 24% | 68% |
Q3KR59 | Rattus norvegicus | 25% | 68% |
Q4Q5F7 | Leishmania major | 92% | 98% |
Q5ZJN4 | Gallus gallus | 24% | 69% |
Q6DIJ4 | Xenopus tropicalis | 25% | 67% |
Q7ZXR7 | Xenopus laevis | 25% | 67% |
Q9FPS3 | Arabidopsis thaliana | 26% | 98% |
V5DHM6 | Trypanosoma cruzi | 41% | 100% |