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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HL22
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 108 | 112 | PF00656 | 0.376 |
CLV_C14_Caspase3-7 | 34 | 38 | PF00656 | 0.488 |
CLV_C14_Caspase3-7 | 6 | 10 | PF00656 | 0.583 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.560 |
CLV_PCSK_FUR_1 | 80 | 84 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 280 | 282 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.555 |
CLV_Separin_Metazoa | 177 | 181 | PF03568 | 0.471 |
DEG_APCC_DBOX_1 | 147 | 155 | PF00400 | 0.598 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.659 |
DEG_SCF_FBW7_1 | 51 | 56 | PF00400 | 0.492 |
DEG_SPOP_SBC_1 | 4 | 8 | PF00917 | 0.534 |
DOC_CKS1_1 | 16 | 21 | PF01111 | 0.522 |
DOC_MAPK_gen_1 | 180 | 187 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 17 | 26 | PF00069 | 0.496 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.526 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.516 |
LIG_14-3-3_CanoR_1 | 148 | 152 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 180 | 186 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 2 | 11 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 229 | 237 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 251 | 259 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 281 | 286 | PF00244 | 0.451 |
LIG_Actin_WH2_2 | 167 | 184 | PF00022 | 0.408 |
LIG_Actin_WH2_2 | 71 | 89 | PF00022 | 0.554 |
LIG_EVH1_1 | 138 | 142 | PF00568 | 0.533 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.524 |
LIG_FHA_2 | 23 | 29 | PF00498 | 0.620 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.520 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.392 |
LIG_Integrin_RGD_1 | 35 | 37 | PF01839 | 0.490 |
LIG_LIR_Gen_1 | 267 | 278 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 246 | 250 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 267 | 273 | PF02991 | 0.583 |
LIG_PCNA_yPIPBox_3 | 115 | 124 | PF02747 | 0.387 |
LIG_PCNA_yPIPBox_3 | 125 | 138 | PF02747 | 0.462 |
LIG_PDZ_Class_3 | 283 | 288 | PF00595 | 0.468 |
LIG_SH2_NCK_1 | 263 | 267 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.398 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.675 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.581 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.406 |
LIG_TRAF2_1 | 274 | 277 | PF00917 | 0.451 |
LIG_WRC_WIRS_1 | 244 | 249 | PF05994 | 0.574 |
MOD_CDK_SPxK_1 | 49 | 55 | PF00069 | 0.510 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.541 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.399 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.617 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.513 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.497 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.613 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.521 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.435 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.612 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.390 |
MOD_GlcNHglycan | 169 | 174 | PF01048 | 0.427 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.443 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.577 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.554 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.437 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.493 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.500 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.400 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.624 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.626 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.610 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.540 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.411 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.390 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.378 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.607 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.547 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.432 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.544 |
MOD_PK_1 | 281 | 287 | PF00069 | 0.452 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.602 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.379 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.558 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.490 |
MOD_PKB_1 | 251 | 259 | PF00069 | 0.490 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.377 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.434 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.500 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.390 |
MOD_Plk_2-3 | 59 | 65 | PF00069 | 0.406 |
MOD_Plk_2-3 | 70 | 76 | PF00069 | 0.354 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.523 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.603 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.496 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.524 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.515 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.510 |
MOD_SUMO_rev_2 | 157 | 167 | PF00179 | 0.507 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 250 | 253 | PF00400 | 0.478 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IEK8 | Leishmania donovani | 57% | 99% |
A4I8K3 | Leishmania infantum | 57% | 99% |
E9B3G3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 99% |
Q4Q4N7 | Leishmania major | 59% | 100% |