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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: Q4Q0E7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.625 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.486 |
DEG_COP1_1 | 53 | 63 | PF00400 | 0.635 |
DEG_SCF_FBW7_1 | 29 | 34 | PF00400 | 0.625 |
DOC_CKS1_1 | 220 | 225 | PF01111 | 0.491 |
DOC_CKS1_1 | 51 | 56 | PF01111 | 0.574 |
DOC_MAPK_gen_1 | 305 | 311 | PF00069 | 0.585 |
DOC_MAPK_RevD_3 | 218 | 234 | PF00069 | 0.623 |
DOC_PP2B_LxvP_1 | 58 | 61 | PF13499 | 0.513 |
DOC_PP4_FxxP_1 | 215 | 218 | PF00568 | 0.512 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.602 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.623 |
LIG_14-3-3_CanoR_1 | 127 | 132 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 142 | 150 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.602 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.663 |
LIG_CaM_IQ_9 | 101 | 116 | PF13499 | 0.478 |
LIG_CaM_IQ_9 | 284 | 300 | PF13499 | 0.484 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.628 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.596 |
LIG_GBD_Chelix_1 | 178 | 186 | PF00786 | 0.437 |
LIG_LIR_Apic_2 | 214 | 218 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 206 | 216 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.585 |
LIG_NRBOX | 114 | 120 | PF00104 | 0.480 |
LIG_PCNA_PIPBox_1 | 169 | 178 | PF02747 | 0.462 |
LIG_PCNA_yPIPBox_3 | 106 | 119 | PF02747 | 0.479 |
LIG_PCNA_yPIPBox_3 | 162 | 176 | PF02747 | 0.468 |
LIG_PTAP_UEV_1 | 254 | 259 | PF05743 | 0.606 |
LIG_SH2_NCK_1 | 209 | 213 | PF00017 | 0.595 |
LIG_SH2_STAP1 | 209 | 213 | PF00017 | 0.595 |
LIG_SH2_STAP1 | 283 | 287 | PF00017 | 0.625 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.493 |
LIG_SH2_STAT3 | 73 | 76 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.494 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.613 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.711 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.468 |
LIG_WRC_WIRS_1 | 212 | 217 | PF05994 | 0.604 |
LIG_WRC_WIRS_1 | 33 | 38 | PF05994 | 0.653 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.652 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.596 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.690 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.602 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.602 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.574 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.691 |
MOD_GlcNHglycan | 204 | 208 | PF01048 | 0.576 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.627 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.598 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.544 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.531 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.736 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.534 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.565 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.673 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.582 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.576 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.560 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.622 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.523 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.562 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.552 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.454 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.553 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.462 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.572 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.615 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.505 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.485 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.482 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.442 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.623 |
MOD_PIKK_1 | 92 | 98 | PF00454 | 0.504 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.424 |
MOD_PKA_1 | 305 | 311 | PF00069 | 0.589 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.671 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.666 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.458 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.646 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.576 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.698 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.509 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.594 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.538 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.572 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.644 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.576 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.622 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.593 |
TRG_ER_diArg_1 | 161 | 163 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 38 | 41 | PF00400 | 0.625 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IK47 | Leishmania donovani | 86% | 99% |
A4IE24 | Leishmania infantum | 86% | 99% |
E9AU48 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |