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: Q4QHS1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 86 | 90 | PF00656 | 0.591 |
CLV_C14_Caspase3-7 | 95 | 99 | PF00656 | 0.477 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.811 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.595 |
CLV_PCSK_FUR_1 | 214 | 218 | PF00082 | 0.590 |
CLV_PCSK_FUR_1 | 34 | 38 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.808 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 204 | 206 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.698 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.585 |
DEG_COP1_1 | 157 | 165 | PF00400 | 0.622 |
DEG_SPOP_SBC_1 | 18 | 22 | PF00917 | 0.644 |
DEG_SPOP_SBC_1 | 223 | 227 | PF00917 | 0.625 |
DEG_SPOP_SBC_1 | 82 | 86 | PF00917 | 0.577 |
DOC_CYCLIN_yCln2_LP_2 | 215 | 221 | PF00134 | 0.564 |
DOC_CYCLIN_yCln2_LP_2 | 52 | 58 | PF00134 | 0.593 |
DOC_MAPK_gen_1 | 204 | 210 | PF00069 | 0.562 |
DOC_PP4_FxxP_1 | 44 | 47 | PF00568 | 0.619 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.801 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.559 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.799 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.653 |
LIG_14-3-3_CanoR_1 | 16 | 25 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 205 | 211 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 246 | 252 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 277 | 286 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 37 | 43 | PF00244 | 0.656 |
LIG_BRCT_BRCA1_1 | 240 | 244 | PF00533 | 0.547 |
LIG_CaM_IQ_9 | 109 | 124 | PF13499 | 0.414 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.439 |
LIG_IBAR_NPY_1 | 54 | 56 | PF08397 | 0.621 |
LIG_LIR_Apic_2 | 41 | 47 | PF02991 | 0.614 |
LIG_NRBOX | 250 | 256 | PF00104 | 0.408 |
LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 197 | 201 | PF00017 | 0.449 |
LIG_SH3_1 | 141 | 147 | PF00018 | 0.579 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.634 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.527 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.698 |
MOD_CDC14_SPxK_1 | 13 | 16 | PF00782 | 0.637 |
MOD_CDC14_SPxK_1 | 170 | 173 | PF00782 | 0.575 |
MOD_CDK_SPK_2 | 167 | 172 | PF00069 | 0.632 |
MOD_CDK_SPxK_1 | 10 | 16 | PF00069 | 0.649 |
MOD_CDK_SPxK_1 | 167 | 173 | PF00069 | 0.595 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.635 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.652 |
MOD_Cter_Amidation | 34 | 37 | PF01082 | 0.633 |
MOD_Cter_Amidation | 69 | 72 | PF01082 | 0.553 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.705 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.633 |
MOD_GlcNHglycan | 240 | 244 | PF01048 | 0.578 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.628 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.648 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.610 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.679 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.498 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.660 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.511 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.656 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.502 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.407 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.541 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.527 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.539 |
MOD_PKA_1 | 230 | 236 | PF00069 | 0.577 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.628 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.633 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.503 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.528 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.408 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.802 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.627 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.652 |
TRG_DiLeu_BaEn_1 | 59 | 64 | PF01217 | 0.619 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.511 |
TRG_ER_diArg_1 | 108 | 111 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 214 | 217 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 277 | 280 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 34 | 37 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 60 | 63 | PF00400 | 0.622 |
TRG_NES_CRM1_1 | 128 | 142 | PF08389 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 117 | 121 | PF00026 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 178 | 182 | PF00026 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQV2 | Leishmania donovani | 90% | 100% |
A4H5T2 | Leishmania braziliensis | 63% | 76% |
A4HU25 | Leishmania infantum | 90% | 100% |
E9AMV5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |