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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QB00
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0008270 | zinc ion binding | 6 | 7 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0046914 | transition metal ion binding | 5 | 7 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 8 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 8 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 22 | 26 | PF00656 | 0.751 |
CLV_C14_Caspase3-7 | 316 | 320 | PF00656 | 0.640 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.606 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.606 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.548 |
DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.620 |
DEG_SPOP_SBC_1 | 398 | 402 | PF00917 | 0.713 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 255 | 264 | PF00134 | 0.601 |
DOC_PP4_FxxP_1 | 371 | 374 | PF00568 | 0.518 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.704 |
DOC_USP7_UBL2_3 | 359 | 363 | PF12436 | 0.580 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.519 |
LIG_14-3-3_CanoR_1 | 6 | 14 | PF00244 | 0.688 |
LIG_Clathr_ClatBox_1 | 287 | 291 | PF01394 | 0.472 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.637 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.383 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.523 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.713 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.730 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.744 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.625 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.502 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.494 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.663 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.756 |
LIG_LIR_Gen_1 | 17 | 26 | PF02991 | 0.602 |
LIG_LIR_Gen_1 | 281 | 290 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.535 |
LIG_SH2_STAP1 | 137 | 141 | PF00017 | 0.690 |
LIG_SH2_STAP1 | 284 | 288 | PF00017 | 0.478 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.700 |
LIG_SUMO_SIM_anti_2 | 213 | 219 | PF11976 | 0.666 |
LIG_SUMO_SIM_par_1 | 285 | 292 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 31 | 38 | PF11976 | 0.700 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.826 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.669 |
LIG_TRAF2_1 | 283 | 286 | PF00917 | 0.479 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.618 |
LIG_WRC_WIRS_1 | 108 | 113 | PF05994 | 0.786 |
MOD_CDK_SPxxK_3 | 223 | 230 | PF00069 | 0.728 |
MOD_CDK_SPxxK_3 | 66 | 73 | PF00069 | 0.514 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.559 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.691 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.437 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.636 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.705 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.483 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.623 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.615 |
MOD_DYRK1A_RPxSP_1 | 66 | 70 | PF00069 | 0.561 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.622 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.681 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.624 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.251 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.289 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.640 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.700 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.741 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.577 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.723 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.526 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.556 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.491 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.564 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.624 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.750 |
MOD_N-GLC_1 | 295 | 300 | PF02516 | 0.574 |
MOD_N-GLC_1 | 382 | 387 | PF02516 | 0.309 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.649 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.636 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.458 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.554 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.509 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.705 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.486 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.689 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.727 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.555 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.555 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.710 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.606 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.547 |
MOD_PKB_1 | 4 | 12 | PF00069 | 0.680 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.724 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.483 |
MOD_Plk_2-3 | 280 | 286 | PF00069 | 0.483 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.685 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.767 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.722 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.665 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.609 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.517 |
TRG_DiLeu_BaEn_2 | 174 | 180 | PF01217 | 0.725 |
TRG_DiLeu_BaEn_4 | 148 | 154 | PF01217 | 0.692 |
TRG_DiLeu_BaEn_4 | 285 | 291 | PF01217 | 0.473 |
TRG_DiLeu_BaLyEn_6 | 216 | 221 | PF01217 | 0.667 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.576 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.757 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.479 |
TRG_NES_CRM1_1 | 88 | 101 | PF08389 | 0.600 |
TRG_NLS_MonoExtN_4 | 2 | 7 | PF00514 | 0.688 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKS7 | Leptomonas seymouri | 44% | 100% |
A0A3Q8IBP7 | Leishmania donovani | 92% | 100% |
A4HD23 | Leishmania braziliensis | 78% | 100% |
A4I0L0 | Leishmania infantum | 93% | 100% |
C9ZVI2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AWH1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |