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: Q4Q9I5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.492 |
CLV_PCSK_FUR_1 | 78 | 82 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.701 |
DEG_APCC_DBOX_1 | 113 | 121 | PF00400 | 0.494 |
DEG_APCC_DBOX_1 | 21 | 29 | PF00400 | 0.440 |
DEG_COP1_1 | 250 | 260 | PF00400 | 0.602 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.552 |
DEG_SPOP_SBC_1 | 277 | 281 | PF00917 | 0.504 |
DOC_PP2B_LxvP_1 | 162 | 165 | PF13499 | 0.492 |
DOC_PP2B_LxvP_1 | 274 | 277 | PF13499 | 0.504 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.537 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 242 | 249 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 36 | 41 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 81 | 87 | PF00244 | 0.469 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.564 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.535 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.493 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.443 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.490 |
LIG_GSK3_LRP6_1 | 163 | 168 | PF00069 | 0.485 |
LIG_LIR_Apic_2 | 207 | 213 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 196 | 205 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.681 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.563 |
LIG_Pex14_1 | 210 | 214 | PF04695 | 0.545 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.437 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.664 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.522 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.602 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.511 |
LIG_SUMO_SIM_anti_2 | 270 | 276 | PF11976 | 0.498 |
LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.613 |
LIG_WRC_WIRS_1 | 226 | 231 | PF05994 | 0.496 |
MOD_CDK_SPxxK_3 | 15 | 22 | PF00069 | 0.474 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.433 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.529 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.500 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.595 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.444 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.495 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.515 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.564 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.538 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.614 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.509 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.552 |
MOD_GlcNHglycan | 6 | 12 | PF01048 | 0.529 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.552 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.606 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.650 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.590 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.478 |
MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.485 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.630 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.611 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.623 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.521 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.520 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.522 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.493 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.524 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.383 |
MOD_PKB_1 | 80 | 88 | PF00069 | 0.473 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.558 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.540 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.587 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.626 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.606 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.508 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.506 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.540 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.520 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.608 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.647 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.478 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 130 | 133 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 187 | 189 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.756 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1M0 | Leptomonas seymouri | 39% | 87% |
A0A3Q8IDN0 | Leishmania donovani | 89% | 100% |
A4HEL4 | Leishmania braziliensis | 64% | 100% |
A4I1U5 | Leishmania infantum | 89% | 100% |
E9AXY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |