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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IBP7
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 | 0.727 |
CLV_C14_Caspase3-7 | 316 | 320 | PF00656 | 0.678 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.663 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.730 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.592 |
DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.601 |
DEG_SPOP_SBC_1 | 394 | 398 | PF00917 | 0.768 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 255 | 264 | PF00134 | 0.665 |
DOC_PP4_FxxP_1 | 367 | 370 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.752 |
DOC_USP7_UBL2_3 | 355 | 359 | PF12436 | 0.608 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.557 |
LIG_14-3-3_CanoR_1 | 6 | 14 | PF00244 | 0.788 |
LIG_Clathr_ClatBox_1 | 287 | 291 | PF01394 | 0.528 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.791 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.430 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.525 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.728 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.733 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.749 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.654 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.565 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.521 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.711 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.813 |
LIG_LIR_Gen_1 | 281 | 290 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.500 |
LIG_SH2_STAP1 | 137 | 141 | PF00017 | 0.736 |
LIG_SH2_STAP1 | 284 | 288 | PF00017 | 0.528 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.753 |
LIG_SUMO_SIM_anti_2 | 213 | 219 | PF11976 | 0.721 |
LIG_SUMO_SIM_par_1 | 19 | 25 | PF11976 | 0.690 |
LIG_SUMO_SIM_par_1 | 285 | 292 | PF11976 | 0.531 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.838 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.731 |
LIG_TRAF2_1 | 283 | 286 | PF00917 | 0.530 |
LIG_WRC_WIRS_1 | 108 | 113 | PF05994 | 0.817 |
MOD_CDK_SPxxK_3 | 223 | 230 | PF00069 | 0.776 |
MOD_CDK_SPxxK_3 | 66 | 73 | PF00069 | 0.548 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.721 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.533 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.483 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.780 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.571 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.686 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.528 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.695 |
MOD_DYRK1A_RPxSP_1 | 66 | 70 | PF00069 | 0.605 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.693 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.737 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.644 |
MOD_GlcNHglycan | 328 | 333 | PF01048 | 0.380 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.317 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.301 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.735 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.754 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.737 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.713 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.559 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.569 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.607 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.795 |
MOD_N-GLC_1 | 295 | 300 | PF02516 | 0.603 |
MOD_N-GLC_1 | 378 | 383 | PF02516 | 0.342 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.770 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.783 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.824 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.623 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.557 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.418 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.773 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.503 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.738 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.793 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.577 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.582 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.782 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.733 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.674 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.593 |
MOD_PKB_1 | 4 | 12 | PF00069 | 0.729 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.729 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.528 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.644 |
MOD_Plk_2-3 | 280 | 286 | PF00069 | 0.538 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.739 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.630 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.808 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.772 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.697 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.607 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.554 |
TRG_DiLeu_BaEn_2 | 174 | 180 | PF01217 | 0.795 |
TRG_DiLeu_BaEn_4 | 148 | 154 | PF01217 | 0.744 |
TRG_DiLeu_BaEn_4 | 285 | 291 | PF01217 | 0.527 |
TRG_DiLeu_BaLyEn_6 | 216 | 221 | PF01217 | 0.716 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.626 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.817 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.494 |
TRG_NLS_MonoExtN_4 | 2 | 7 | PF00514 | 0.732 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKS7 | Leptomonas seymouri | 45% | 100% |
A4HD23 | Leishmania braziliensis | 79% | 100% |
A4I0L0 | Leishmania infantum | 99% | 100% |
C9ZVI2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AWH1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QB00 | Leishmania major | 92% | 100% |