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: A0A3S7X1A2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 147 | 153 | PF00089 | 0.442 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.534 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 88 | 90 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.427 |
DEG_APCC_DBOX_1 | 174 | 182 | PF00400 | 0.520 |
DEG_APCC_KENBOX_2 | 106 | 110 | PF00400 | 0.517 |
DOC_CDC14_PxL_1 | 43 | 51 | PF14671 | 0.556 |
DOC_CKS1_1 | 90 | 95 | PF01111 | 0.434 |
DOC_MAPK_MEF2A_6 | 56 | 63 | PF00069 | 0.579 |
DOC_PP1_RVXF_1 | 120 | 127 | PF00149 | 0.484 |
DOC_PP4_FxxP_1 | 90 | 93 | PF00568 | 0.464 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.444 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.517 |
LIG_14-3-3_CanoR_1 | 128 | 133 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 150 | 156 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 185 | 189 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 89 | 93 | PF00244 | 0.600 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.625 |
LIG_Clathr_ClatBox_1 | 136 | 140 | PF01394 | 0.490 |
LIG_DLG_GKlike_1 | 128 | 136 | PF00625 | 0.462 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.497 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.507 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.469 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.417 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.543 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.594 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.610 |
LIG_GBD_Chelix_1 | 102 | 110 | PF00786 | 0.400 |
LIG_LIR_Gen_1 | 131 | 139 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.457 |
LIG_PDZ_Class_2 | 185 | 190 | PF00595 | 0.451 |
LIG_Pex14_2 | 133 | 137 | PF04695 | 0.435 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.668 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.544 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.587 |
LIG_SUMO_SIM_anti_2 | 38 | 44 | PF11976 | 0.551 |
LIG_TRAF2_1 | 10 | 13 | PF00917 | 0.555 |
LIG_TRAF2_1 | 138 | 141 | PF00917 | 0.611 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.527 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.504 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.572 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.588 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.475 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.579 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.500 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.561 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.575 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.539 |
MOD_GlcNHglycan | 80 | 84 | PF01048 | 0.556 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.462 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.463 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.461 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.516 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.567 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.694 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.419 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.480 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.485 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.660 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.613 |
MOD_PK_1 | 155 | 161 | PF00069 | 0.406 |
MOD_PKA_1 | 128 | 134 | PF00069 | 0.462 |
MOD_PKA_1 | 88 | 94 | PF00069 | 0.578 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.462 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.457 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.441 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.606 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.467 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.663 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.505 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.516 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.508 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.654 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.507 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 174 | 177 | PF00400 | 0.535 |
TRG_NES_CRM1_1 | 104 | 118 | PF08389 | 0.539 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7T0 | Leptomonas seymouri | 41% | 95% |
A4HGB9 | Leishmania braziliensis | 70% | 100% |
E9ADJ8 | Leishmania major | 85% | 100% |
E9AHH7 | Leishmania infantum | 98% | 100% |
E9AZP0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |