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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4Q8Z4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.604 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.633 |
CLV_PCSK_FUR_1 | 132 | 136 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.590 |
DOC_CKS1_1 | 48 | 53 | PF01111 | 0.755 |
DOC_MAPK_gen_1 | 112 | 122 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 161 | 170 | PF00069 | 0.553 |
DOC_MAPK_gen_1 | 181 | 189 | PF00069 | 0.600 |
DOC_MAPK_gen_1 | 32 | 38 | PF00069 | 0.691 |
DOC_MAPK_HePTP_8 | 160 | 172 | PF00069 | 0.603 |
DOC_MAPK_MEF2A_6 | 163 | 172 | PF00069 | 0.601 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.706 |
DOC_USP7_UBL2_3 | 129 | 133 | PF12436 | 0.537 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 17 | 22 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 24 | 29 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 32 | 37 | PF00244 | 0.589 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.713 |
LIG_CSL_BTD_1 | 8 | 11 | PF09270 | 0.713 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.689 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.607 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.791 |
LIG_LIR_Gen_1 | 125 | 131 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.688 |
LIG_PDZ_Class_2 | 201 | 206 | PF00595 | 0.615 |
LIG_SH2_CRK | 192 | 196 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.623 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.721 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.590 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.529 |
LIG_SUMO_SIM_par_1 | 96 | 102 | PF11976 | 0.683 |
LIG_WRC_WIRS_1 | 201 | 206 | PF05994 | 0.650 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.745 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.647 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.596 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.728 |
MOD_Cter_Amidation | 30 | 33 | PF01082 | 0.755 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.547 |
MOD_GlcNHglycan | 55 | 59 | PF01048 | 0.791 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.734 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.589 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.290 |
MOD_N-GLC_2 | 165 | 167 | PF02516 | 0.397 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.633 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.504 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.560 |
MOD_PK_1 | 17 | 23 | PF00069 | 0.743 |
MOD_PKA_1 | 17 | 23 | PF00069 | 0.546 |
MOD_PKA_1 | 24 | 30 | PF00069 | 0.604 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.711 |
MOD_PKA_1 | 32 | 38 | PF00069 | 0.608 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.606 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.554 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.557 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.598 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.711 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.589 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.552 |
MOD_Plk_2-3 | 64 | 70 | PF00069 | 0.557 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.601 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.495 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.647 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.681 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.644 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.576 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 158 | 160 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.605 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P8F5 | Trypanosomatidae | 23% | 91% |
A0A1X0P8T2 | Trypanosomatidae | 25% | 91% |
A0A3Q8IPD3 | Leishmania donovani | 90% | 100% |
A4HF42 | Leishmania braziliensis | 70% | 94% |
A4I2C6 | Leishmania infantum | 90% | 100% |
E9AYH8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |