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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 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: E9AI41
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.516 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.571 |
DEG_APCC_DBOX_1 | 138 | 146 | PF00400 | 0.371 |
DOC_MAPK_gen_1 | 139 | 147 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 141 | 149 | PF00069 | 0.371 |
DOC_PP1_RVXF_1 | 238 | 245 | PF00149 | 0.414 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.651 |
DOC_USP7_UBL2_3 | 15 | 19 | PF12436 | 0.573 |
DOC_USP7_UBL2_3 | 44 | 48 | PF12436 | 0.403 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.679 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.495 |
LIG_14-3-3_CanoR_1 | 168 | 176 | PF00244 | 0.431 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.463 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.393 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.337 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.381 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.627 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.561 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.496 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.531 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.536 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.448 |
LIG_LIR_Gen_1 | 187 | 195 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.449 |
LIG_NRBOX | 141 | 147 | PF00104 | 0.420 |
LIG_NRBOX | 216 | 222 | PF00104 | 0.479 |
LIG_Pex14_2 | 189 | 193 | PF04695 | 0.358 |
LIG_Pex14_2 | 259 | 263 | PF04695 | 0.483 |
LIG_REV1ctd_RIR_1 | 242 | 251 | PF16727 | 0.423 |
LIG_SH2_STAT3 | 157 | 160 | PF00017 | 0.478 |
LIG_SH2_STAT3 | 32 | 35 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.473 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.574 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.370 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.467 |
LIG_SH3_4 | 6 | 13 | PF00018 | 0.631 |
LIG_SUMO_SIM_par_1 | 198 | 203 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 65 | 71 | PF11976 | 0.476 |
MOD_CDC14_SPxK_1 | 71 | 74 | PF00782 | 0.505 |
MOD_CDK_SPK_2 | 232 | 237 | PF00069 | 0.380 |
MOD_CDK_SPxK_1 | 68 | 74 | PF00069 | 0.497 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.597 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.507 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.397 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.487 |
MOD_Cter_Amidation | 12 | 15 | PF01082 | 0.663 |
MOD_Cter_Amidation | 17 | 20 | PF01082 | 0.622 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.534 |
MOD_GlcNHglycan | 194 | 198 | PF01048 | 0.271 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.567 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.517 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.409 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.558 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.391 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.644 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.660 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.479 |
MOD_N-GLC_1 | 204 | 209 | PF02516 | 0.440 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.446 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.555 |
MOD_PIKK_1 | 115 | 121 | PF00454 | 0.637 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.434 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.652 |
MOD_PK_1 | 172 | 178 | PF00069 | 0.455 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.525 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.482 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.536 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.592 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.431 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.412 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.536 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.467 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.497 |
TRG_NLS_MonoExtC_3 | 46 | 52 | PF00514 | 0.384 |
TRG_NLS_MonoExtN_4 | 12 | 18 | PF00514 | 0.591 |
TRG_NLS_MonoExtN_4 | 44 | 51 | PF00514 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 153 | 158 | PF00026 | 0.373 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKR2 | Leptomonas seymouri | 45% | 100% |
A0A3Q8I8T9 | Leishmania donovani | 75% | 100% |
A0A3R7KUI1 | Trypanosoma rangeli | 27% | 87% |
A4H651 | Leishmania braziliensis | 98% | 100% |
A4HUH1 | Leishmania infantum | 74% | 100% |
C9ZVJ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 92% |
E9AN69 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4QHF6 | Leishmania major | 73% | 100% |
V5B6H6 | Trypanosoma cruzi | 25% | 86% |