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:0005739 | mitochondrion | 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 | 4 |
GO:0016020 | membrane | 2 | 3 |
Related structures:
AlphaFold database: A0A3Q8IC90
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 77 | 81 | PF00656 | 0.493 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.619 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 222 | 224 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.524 |
DOC_CYCLIN_RxL_1 | 139 | 149 | PF00134 | 0.485 |
DOC_PP1_RVXF_1 | 220 | 227 | PF00149 | 0.606 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.501 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.586 |
LIG_14-3-3_CanoR_1 | 74 | 79 | PF00244 | 0.523 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.436 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.719 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.555 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.545 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.516 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.631 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.399 |
LIG_LIR_Gen_1 | 172 | 181 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 207 | 215 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 172 | 177 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 89 | 93 | PF02991 | 0.459 |
LIG_NRBOX | 245 | 251 | PF00104 | 0.480 |
LIG_SH2_CRK | 174 | 178 | PF00017 | 0.438 |
LIG_SH2_CRK | 247 | 251 | PF00017 | 0.433 |
LIG_SH2_CRK | 30 | 34 | PF00017 | 0.474 |
LIG_SH2_SRC | 78 | 81 | PF00017 | 0.568 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.457 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.503 |
LIG_SUMO_SIM_anti_2 | 100 | 107 | PF11976 | 0.457 |
LIG_SUMO_SIM_anti_2 | 47 | 53 | PF11976 | 0.610 |
LIG_SUMO_SIM_par_1 | 113 | 121 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 143 | 149 | PF11976 | 0.544 |
LIG_ULM_U2AF65_1 | 222 | 227 | PF00076 | 0.612 |
LIG_WRC_WIRS_1 | 212 | 217 | PF05994 | 0.558 |
MOD_CDK_SPxK_1 | 157 | 163 | PF00069 | 0.533 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.580 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.689 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.670 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.616 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.574 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.587 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.492 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.679 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.696 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.674 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.466 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.421 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.552 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.502 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.692 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.504 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.495 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.648 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.659 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.502 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.446 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.583 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.504 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.459 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.551 |
MOD_PKA_1 | 74 | 80 | PF00069 | 0.514 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.574 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.514 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.468 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.419 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.409 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.468 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.545 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.583 |
MOD_SUMO_rev_2 | 118 | 125 | PF00179 | 0.515 |
TRG_DiLeu_BaEn_1 | 143 | 148 | PF01217 | 0.541 |
TRG_DiLeu_BaEn_1 | 47 | 52 | PF01217 | 0.607 |
TRG_DiLeu_BaLyEn_6 | 142 | 147 | PF01217 | 0.494 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.478 |
TRG_NLS_MonoExtN_4 | 219 | 226 | PF00514 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 123 | 127 | PF00026 | 0.591 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8E4 | Leptomonas seymouri | 57% | 100% |
A0A1X0NTC5 | Trypanosomatidae | 38% | 100% |
A0A3R7NDY8 | Trypanosoma rangeli | 36% | 100% |
A4HCE9 | Leishmania braziliensis | 81% | 100% |
A4HZY0 | Leishmania infantum | 99% | 100% |
C9ZSL9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AVU0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QBN9 | Leishmania major | 92% | 100% |
V5BVV8 | Trypanosoma cruzi | 35% | 100% |