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: A0A3S5H5M8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.741 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.406 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.463 |
CLV_PCSK_PC1ET2_1 | 155 | 157 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.414 |
DEG_APCC_DBOX_1 | 217 | 225 | PF00400 | 0.498 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.691 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.626 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.558 |
DOC_USP7_UBL2_3 | 129 | 133 | PF12436 | 0.455 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.617 |
LIG_14-3-3_CanoR_1 | 182 | 192 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 278 | 285 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 88 | 94 | PF00244 | 0.474 |
LIG_Actin_WH2_2 | 14 | 29 | PF00022 | 0.450 |
LIG_Actin_WH2_2 | 204 | 222 | PF00022 | 0.482 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.594 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.477 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.621 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.444 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.513 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.468 |
LIG_PCNA_yPIPBox_3 | 91 | 104 | PF02747 | 0.468 |
LIG_SH2_NCK_1 | 176 | 180 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 119 | 123 | PF00017 | 0.454 |
LIG_SH2_STAT3 | 119 | 122 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.484 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.668 |
LIG_TRAF2_1 | 206 | 209 | PF00917 | 0.517 |
LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.566 |
LIG_UBA3_1 | 160 | 166 | PF00899 | 0.416 |
LIG_UBA3_1 | 34 | 40 | PF00899 | 0.433 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.479 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.531 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.450 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.588 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.516 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.679 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.492 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.549 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.516 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.443 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.689 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.532 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.366 |
MOD_Cter_Amidation | 72 | 75 | PF01082 | 0.529 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.446 |
MOD_GlcNHglycan | 172 | 176 | PF01048 | 0.457 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.647 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.591 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.642 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.584 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.425 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.563 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.597 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.690 |
MOD_LATS_1 | 276 | 282 | PF00433 | 0.530 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.576 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.601 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.434 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.642 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.553 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.456 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.544 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.553 |
MOD_PKA_1 | 74 | 80 | PF00069 | 0.502 |
MOD_PKA_1 | 98 | 104 | PF00069 | 0.466 |
MOD_PKB_1 | 87 | 95 | PF00069 | 0.499 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.577 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.422 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.511 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.519 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.636 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.620 |
MOD_SUMO_rev_2 | 94 | 100 | PF00179 | 0.484 |
TRG_ER_diArg_1 | 167 | 169 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 197 | 199 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 218 | 221 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.371 |
TRG_Pf-PMV_PEXEL_1 | 278 | 282 | PF00026 | 0.590 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3D4 | Leptomonas seymouri | 39% | 80% |
A4H4H4 | Leishmania braziliensis | 68% | 100% |
A4HSP9 | Leishmania infantum | 99% | 100% |
E9AKN4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QJ73 | Leishmania major | 86% | 100% |