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: E9AMY9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.728 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.745 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.514 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.591 |
CLV_PCSK_PC7_1 | 225 | 231 | PF00082 | 0.584 |
CLV_PCSK_PC7_1 | 244 | 250 | PF00082 | 0.643 |
CLV_PCSK_PC7_1 | 99 | 105 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.381 |
DEG_APCC_DBOX_1 | 214 | 222 | PF00400 | 0.588 |
DOC_CKS1_1 | 240 | 245 | PF01111 | 0.521 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.695 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.416 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.717 |
LIG_14-3-3_CanoR_1 | 104 | 113 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 138 | 144 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 215 | 219 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 230 | 235 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 248 | 257 | PF00244 | 0.632 |
LIG_Actin_WH2_2 | 217 | 234 | PF00022 | 0.584 |
LIG_BIR_III_4 | 17 | 21 | PF00653 | 0.598 |
LIG_Clathr_ClatBox_1 | 112 | 116 | PF01394 | 0.544 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.484 |
LIG_LIR_Apic_2 | 191 | 196 | PF02991 | 0.720 |
LIG_SH2_CRK | 193 | 197 | PF00017 | 0.721 |
LIG_SUMO_SIM_par_1 | 111 | 118 | PF11976 | 0.610 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.544 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.578 |
MOD_CDC14_SPxK_1 | 11 | 14 | PF00782 | 0.603 |
MOD_CDK_SPK_2 | 175 | 180 | PF00069 | 0.598 |
MOD_CDK_SPK_2 | 239 | 244 | PF00069 | 0.616 |
MOD_CDK_SPxK_1 | 184 | 190 | PF00069 | 0.598 |
MOD_CDK_SPxK_1 | 8 | 14 | PF00069 | 0.600 |
MOD_CDK_SPxxK_3 | 192 | 199 | PF00069 | 0.618 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.619 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.478 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.574 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.519 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.590 |
MOD_GlcNHglycan | 116 | 120 | PF01048 | 0.586 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.595 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.601 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.518 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.486 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.635 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.462 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.633 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.634 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.415 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.460 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.438 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.713 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.734 |
MOD_PK_1 | 230 | 236 | PF00069 | 0.608 |
MOD_PKA_1 | 201 | 207 | PF00069 | 0.687 |
MOD_PKA_1 | 248 | 254 | PF00069 | 0.739 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.606 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.747 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.590 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.580 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.640 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.385 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.509 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.567 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.693 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.621 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.542 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.639 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.638 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.720 |
TRG_DiLeu_BaLyEn_6 | 35 | 40 | PF01217 | 0.672 |
TRG_ER_diArg_1 | 103 | 105 | PF00400 | 0.413 |
TRG_NLS_MonoExtN_4 | 99 | 106 | PF00514 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 82 | 87 | PF00026 | 0.437 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8A2 | Leptomonas seymouri | 47% | 97% |
A0A3S5H6E8 | Leishmania donovani | 87% | 100% |
A4H5W4 | Leishmania braziliensis | 69% | 100% |
A4HU59 | Leishmania infantum | 88% | 100% |
Q4QHN8 | Leishmania major | 88% | 100% |