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: 1 |
NetGPI | no | yes: 0, no: 1 |
Related structures:
AlphaFold database: A0A3S5H5V1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.485 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.433 |
CLV_PCSK_PC7_1 | 134 | 140 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.434 |
DOC_CYCLIN_yCln2_LP_2 | 126 | 132 | PF00134 | 0.473 |
DOC_PP1_RVXF_1 | 136 | 143 | PF00149 | 0.431 |
DOC_PP2B_LxvP_1 | 126 | 129 | PF13499 | 0.488 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.423 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.497 |
LIG_14-3-3_CanoR_1 | 41 | 47 | PF00244 | 0.500 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.497 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.502 |
LIG_SH2_STAT3 | 93 | 96 | PF00017 | 0.434 |
LIG_SH3_2 | 129 | 134 | PF14604 | 0.454 |
LIG_SH3_2 | 29 | 34 | PF14604 | 0.487 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.473 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.485 |
LIG_SH3_CIN85_PxpxPR_1 | 29 | 34 | PF14604 | 0.487 |
LIG_WW_3 | 131 | 135 | PF00397 | 0.444 |
LIG_WW_3 | 31 | 35 | PF00397 | 0.496 |
MOD_CAAXbox | 171 | 174 | PF01239 | 0.430 |
MOD_CDC14_SPxK_1 | 131 | 134 | PF00782 | 0.445 |
MOD_CDK_SPxK_1 | 128 | 134 | PF00069 | 0.456 |
MOD_CDK_SPxxK_3 | 27 | 34 | PF00069 | 0.486 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.459 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.415 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.470 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.503 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.428 |
MOD_Cter_Amidation | 1 | 4 | PF01082 | 0.495 |
MOD_Cter_Amidation | 136 | 139 | PF01082 | 0.429 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.507 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.429 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.450 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.427 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.506 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.484 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.483 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.504 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.446 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.498 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.494 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.431 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.506 |
MOD_N-GLC_1 | 41 | 46 | PF02516 | 0.502 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.447 |
MOD_N-GLC_1 | 99 | 104 | PF02516 | 0.441 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.502 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.444 |
MOD_PKA_1 | 4 | 10 | PF00069 | 0.488 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.435 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.503 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.488 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.504 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.456 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.502 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.486 |
MOD_SUMO_rev_2 | 110 | 119 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 150 | 158 | PF00179 | 0.473 |
MOD_SUMO_rev_2 | 49 | 55 | PF00179 | 0.495 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.489 |