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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4H385
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 5 | 9 | PF00656 | 0.495 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.552 |
DEG_SCF_FBW7_1 | 146 | 153 | PF00400 | 0.694 |
DOC_CKS1_1 | 123 | 128 | PF01111 | 0.664 |
DOC_CKS1_1 | 147 | 152 | PF01111 | 0.696 |
DOC_CYCLIN_yClb3_PxF_3 | 150 | 156 | PF00134 | 0.600 |
DOC_PP1_RVXF_1 | 14 | 20 | PF00149 | 0.538 |
DOC_PP4_FxxP_1 | 19 | 22 | PF00568 | 0.515 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.775 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.574 |
LIG_14-3-3_CanoR_1 | 107 | 111 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 16 | 22 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 268 | 277 | PF00244 | 0.593 |
LIG_BRCT_BRCA1_1 | 273 | 277 | PF00533 | 0.578 |
LIG_EVH1_1 | 231 | 235 | PF00568 | 0.527 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.502 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.488 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.716 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.589 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.665 |
LIG_LIR_Gen_1 | 131 | 137 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 169 | 179 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 274 | 280 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 8 | 18 | PF02991 | 0.443 |
LIG_LIR_LC3C_4 | 12 | 15 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.719 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 274 | 280 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 8 | 13 | PF02991 | 0.438 |
LIG_PDZ_Class_3 | 275 | 280 | PF00595 | 0.639 |
LIG_SH3_1 | 148 | 154 | PF00018 | 0.533 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.696 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.591 |
LIG_SUMO_SIM_par_1 | 112 | 119 | PF11976 | 0.605 |
LIG_SUMO_SIM_par_1 | 211 | 219 | PF11976 | 0.506 |
LIG_TRAF2_1 | 175 | 178 | PF00917 | 0.582 |
LIG_WRC_WIRS_1 | 168 | 173 | PF05994 | 0.530 |
LIG_WW_3 | 145 | 149 | PF00397 | 0.539 |
MOD_CDK_SPK_2 | 122 | 127 | PF00069 | 0.672 |
MOD_CDK_SPxK_1 | 142 | 148 | PF00069 | 0.533 |
MOD_CDK_SPxK_1 | 220 | 226 | PF00069 | 0.639 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.600 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.615 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.558 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.655 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.662 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.740 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.614 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.602 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.503 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.586 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.697 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.658 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.624 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.656 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.765 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.625 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.627 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.684 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.516 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.653 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.618 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.599 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.714 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.777 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.696 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.674 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.590 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.677 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.562 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.687 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.591 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.610 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.649 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.585 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.665 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.675 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.635 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.493 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.599 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.760 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.693 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.623 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.560 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.524 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.535 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.684 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.610 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.576 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.577 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.675 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.527 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.550 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.599 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.483 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.589 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.753 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.620 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.718 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.563 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.533 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.573 |
TRG_DiLeu_BaEn_1 | 56 | 61 | PF01217 | 0.500 |
TRG_DiLeu_BaEn_4 | 56 | 62 | PF01217 | 0.500 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I318 | Leptomonas seymouri | 41% | 86% |
A0A3S5H4W5 | Leishmania donovani | 70% | 93% |
A4HRJ0 | Leishmania infantum | 70% | 93% |
E9AC58 | Leishmania major | 67% | 99% |
E9AJF4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 97% |