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:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0020023 | kinetoplast | 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 |
Related structures:
AlphaFold database: E9AWJ9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.535 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 116 | 118 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.393 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.550 |
DOC_CDC14_PxL_1 | 147 | 155 | PF14671 | 0.282 |
DOC_CYCLIN_RxL_1 | 30 | 39 | PF00134 | 0.648 |
DOC_MAPK_gen_1 | 215 | 221 | PF00069 | 0.687 |
DOC_PP1_RVXF_1 | 216 | 222 | PF00149 | 0.661 |
DOC_USP7_UBL2_3 | 165 | 169 | PF12436 | 0.297 |
DOC_USP7_UBL2_3 | 242 | 246 | PF12436 | 0.578 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.282 |
LIG_14-3-3_CanoR_1 | 10 | 20 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 158 | 162 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.346 |
LIG_Actin_WH2_2 | 193 | 210 | PF00022 | 0.546 |
LIG_APCC_ABBAyCdc20_2 | 158 | 164 | PF00400 | 0.296 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.278 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.401 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.323 |
LIG_Pex14_2 | 188 | 192 | PF04695 | 0.306 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.340 |
LIG_SH2_CRK | 32 | 36 | PF00017 | 0.636 |
LIG_SH2_CRK | 70 | 74 | PF00017 | 0.273 |
LIG_SH2_CRK | 97 | 101 | PF00017 | 0.269 |
LIG_SH2_GRB2like | 63 | 66 | PF00017 | 0.335 |
LIG_SH2_NCK_1 | 138 | 142 | PF00017 | 0.340 |
LIG_SH2_PTP2 | 99 | 102 | PF00017 | 0.269 |
LIG_SH2_SRC | 224 | 227 | PF00017 | 0.741 |
LIG_SH2_SRC | 99 | 102 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 105 | 109 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.269 |
LIG_SH3_1 | 224 | 230 | PF00018 | 0.713 |
LIG_SH3_2 | 230 | 235 | PF14604 | 0.734 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.672 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.668 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.447 |
LIG_TYR_ITIM | 95 | 100 | PF00017 | 0.282 |
LIG_UBA3_1 | 89 | 94 | PF00899 | 0.296 |
MOD_CDC14_SPxK_1 | 127 | 130 | PF00782 | 0.282 |
MOD_CDK_SPxK_1 | 124 | 130 | PF00069 | 0.282 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.284 |
MOD_Cter_Amidation | 114 | 117 | PF01082 | 0.491 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.428 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.482 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.391 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.502 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.286 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.282 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.282 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.544 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.362 |
MOD_PKA_1 | 24 | 30 | PF00069 | 0.687 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.275 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.285 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.282 |
MOD_Plk_2-3 | 139 | 145 | PF00069 | 0.313 |
MOD_Plk_2-3 | 177 | 183 | PF00069 | 0.282 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.282 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.282 |
MOD_SUMO_for_1 | 107 | 110 | PF00179 | 0.334 |
MOD_SUMO_rev_2 | 160 | 168 | PF00179 | 0.348 |
TRG_DiLeu_BaLyEn_6 | 190 | 195 | PF01217 | 0.378 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.586 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.259 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.282 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.622 |
TRG_NLS_MonoExtN_4 | 213 | 219 | PF00514 | 0.665 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P429 | Leptomonas seymouri | 86% | 100% |
A0A0S4J094 | Bodo saltans | 68% | 100% |
A0A1X0NJD4 | Trypanosomatidae | 76% | 100% |
A0A3R7KS59 | Trypanosoma rangeli | 73% | 100% |
A0A3S7WXZ8 | Leishmania donovani | 95% | 100% |
A4HD67 | Leishmania braziliensis | 91% | 100% |
D0A6Y0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 73% | 100% |
E9AH21 | Leishmania infantum | 94% | 100% |
Q4QAX1 | Leishmania major | 96% | 100% |