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: E9ASY6
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016407 | acetyltransferase activity | 5 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016746 | acyltransferase activity | 3 | 9 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.736 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.698 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.538 |
DEG_APCC_DBOX_1 | 349 | 357 | PF00400 | 0.387 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.514 |
DEG_SPOP_SBC_1 | 113 | 117 | PF00917 | 0.622 |
DOC_CYCLIN_yCln2_LP_2 | 361 | 367 | PF00134 | 0.317 |
DOC_MAPK_gen_1 | 161 | 169 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 291 | 299 | PF00069 | 0.449 |
DOC_PP1_RVXF_1 | 294 | 300 | PF00149 | 0.376 |
DOC_PP1_RVXF_1 | 56 | 63 | PF00149 | 0.543 |
DOC_PP4_FxxP_1 | 174 | 177 | PF00568 | 0.393 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.578 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.685 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.739 |
LIG_14-3-3_CanoR_1 | 12 | 18 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 125 | 133 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 184 | 189 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 209 | 217 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 7 | 11 | PF00244 | 0.576 |
LIG_BRCT_BRCA1_1 | 170 | 174 | PF00533 | 0.390 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.457 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.386 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.426 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.575 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.466 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.540 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.400 |
LIG_LIR_Apic_2 | 171 | 177 | PF02991 | 0.390 |
LIG_LIR_Apic_2 | 49 | 53 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 229 | 239 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 267 | 275 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 139 | 144 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 267 | 271 | PF02991 | 0.318 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 170 | 174 | PF00017 | 0.276 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 46 | 50 | PF00017 | 0.445 |
LIG_SH2_STAT3 | 150 | 153 | PF00017 | 0.479 |
LIG_SH2_STAT3 | 170 | 173 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.382 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.406 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.391 |
LIG_SUMO_SIM_par_1 | 164 | 172 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 184 | 190 | PF11976 | 0.612 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.572 |
LIG_TRAF2_1 | 212 | 215 | PF00917 | 0.429 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.599 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.487 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.702 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.578 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.544 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.753 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.570 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.416 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.425 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.794 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.506 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.327 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.728 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.624 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.770 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.802 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.675 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.634 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.543 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.690 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.380 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.395 |
MOD_N-GLC_1 | 323 | 328 | PF02516 | 0.544 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.662 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.480 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.470 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.561 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.321 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.510 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.606 |
MOD_NEK2_2 | 13 | 18 | PF00069 | 0.601 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.438 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.600 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.431 |
MOD_PKA_1 | 198 | 204 | PF00069 | 0.528 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.575 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.585 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.530 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.602 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.582 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.664 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.313 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.499 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.498 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.591 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.690 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.737 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_4 | 164 | 170 | PF01217 | 0.500 |
TRG_DiLeu_BaLyEn_6 | 128 | 133 | PF01217 | 0.562 |
TRG_DiLeu_BaLyEn_6 | 248 | 253 | PF01217 | 0.336 |
TRG_DiLeu_BaLyEn_6 | 55 | 60 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.351 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 197 | 200 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 332 | 334 | PF00400 | 0.666 |
TRG_NLS_MonoExtN_4 | 195 | 201 | PF00514 | 0.596 |
TRG_Pf-PMV_PEXEL_1 | 209 | 214 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9D4 | Leptomonas seymouri | 69% | 99% |
A0A0S4IZI8 | Bodo saltans | 38% | 86% |
A0A1X0P7V3 | Trypanosomatidae | 45% | 100% |
A0A3R7K298 | Trypanosoma rangeli | 46% | 100% |
A0A3S7XAU7 | Leishmania donovani | 94% | 100% |
A4HP78 | Leishmania braziliensis | 87% | 100% |
A4IDI3 | Leishmania infantum | 94% | 100% |
D0A374 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
Q4Q1L2 | Leishmania major | 91% | 100% |
V5DCI4 | Trypanosoma cruzi | 45% | 100% |