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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HP78
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0016407 | acetyltransferase activity | 5 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016746 | acyltransferase activity | 3 | 8 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.547 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 199 | 201 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.570 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.551 |
DOC_CYCLIN_yCln2_LP_2 | 362 | 368 | PF00134 | 0.364 |
DOC_MAPK_gen_1 | 162 | 170 | PF00069 | 0.419 |
DOC_MAPK_gen_1 | 292 | 300 | PF00069 | 0.494 |
DOC_PP1_RVXF_1 | 295 | 301 | PF00149 | 0.426 |
DOC_PP1_RVXF_1 | 56 | 63 | PF00149 | 0.575 |
DOC_PP4_FxxP_1 | 175 | 178 | PF00568 | 0.443 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.611 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.682 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.726 |
LIG_14-3-3_CanoR_1 | 126 | 134 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 185 | 190 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 210 | 218 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 7 | 11 | PF00244 | 0.584 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.511 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.400 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.397 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.300 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.587 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.342 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.532 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.626 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.552 |
LIG_LIR_Apic_2 | 173 | 178 | PF02991 | 0.443 |
LIG_LIR_Apic_2 | 49 | 53 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 230 | 240 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 268 | 276 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 268 | 272 | PF02991 | 0.385 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 171 | 175 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 46 | 50 | PF00017 | 0.501 |
LIG_SH2_STAT3 | 171 | 174 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.432 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.600 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.435 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.416 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.608 |
LIG_SUMO_SIM_par_1 | 185 | 192 | PF11976 | 0.622 |
LIG_TRAF2_1 | 137 | 140 | PF00917 | 0.602 |
LIG_TRAF2_1 | 163 | 166 | PF00917 | 0.309 |
LIG_TRAF2_1 | 213 | 216 | PF00917 | 0.553 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.622 |
LIG_TYR_ITIM | 316 | 321 | PF00017 | 0.509 |
MOD_CDK_SPK_2 | 104 | 109 | PF00069 | 0.529 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.642 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.434 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.553 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.625 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.729 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.585 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.439 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.425 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.565 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.520 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.370 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.724 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.682 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.740 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.668 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.572 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.555 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.554 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.490 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.482 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.371 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.495 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.687 |
MOD_NEK2_2 | 13 | 18 | PF00069 | 0.637 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.488 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.472 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.519 |
MOD_PKA_1 | 199 | 205 | PF00069 | 0.559 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.622 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.594 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.559 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.592 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.779 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.367 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.470 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.526 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.587 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.541 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.700 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.726 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.515 |
TRG_DiLeu_BaEn_4 | 165 | 171 | PF01217 | 0.517 |
TRG_DiLeu_BaLyEn_6 | 129 | 134 | PF01217 | 0.598 |
TRG_DiLeu_BaLyEn_6 | 249 | 254 | PF01217 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 55 | 60 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.533 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.727 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.525 |
TRG_NES_CRM1_1 | 352 | 363 | PF08389 | 0.300 |
TRG_NLS_MonoExtN_4 | 196 | 202 | PF00514 | 0.629 |
TRG_Pf-PMV_PEXEL_1 | 210 | 215 | PF00026 | 0.502 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9D4 | Leptomonas seymouri | 70% | 99% |
A0A0S4IZI8 | Bodo saltans | 39% | 86% |
A0A1X0P7V3 | Trypanosomatidae | 50% | 100% |
A0A3R7K298 | Trypanosoma rangeli | 45% | 100% |
A0A3S7XAU7 | Leishmania donovani | 88% | 100% |
A4IDI3 | Leishmania infantum | 88% | 100% |
D0A374 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9ASY6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q1L2 | Leishmania major | 85% | 100% |
V5DCI4 | Trypanosoma cruzi | 45% | 100% |