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: Q4Q167
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.504 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 104 | 106 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 131 | 133 | PF00082 | 0.456 |
CLV_PCSK_PC1ET2_1 | 43 | 45 | PF00082 | 0.500 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.681 |
DOC_MAPK_DCC_7 | 15 | 25 | PF00069 | 0.515 |
DOC_MAPK_gen_1 | 131 | 139 | PF00069 | 0.609 |
DOC_MAPK_MEF2A_6 | 131 | 139 | PF00069 | 0.532 |
DOC_MAPK_NFAT4_5 | 132 | 140 | PF00069 | 0.494 |
DOC_PIKK_1 | 64 | 72 | PF02985 | 0.545 |
DOC_PP2B_LxvP_1 | 154 | 157 | PF13499 | 0.694 |
DOC_PP2B_LxvP_1 | 160 | 163 | PF13499 | 0.665 |
DOC_PP2B_PxIxI_1 | 33 | 39 | PF00149 | 0.522 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.640 |
DOC_USP7_UBL2_3 | 43 | 47 | PF12436 | 0.562 |
LIG_14-3-3_CanoR_1 | 132 | 136 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 50 | 56 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 94 | 100 | PF00244 | 0.686 |
LIG_Actin_WH2_2 | 122 | 138 | PF00022 | 0.489 |
LIG_EVH1_1 | 160 | 164 | PF00568 | 0.646 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.626 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.588 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.603 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.635 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.566 |
LIG_PCNA_yPIPBox_3 | 105 | 119 | PF02747 | 0.522 |
LIG_SH2_SRC | 75 | 78 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.542 |
LIG_SH3_1 | 158 | 164 | PF00018 | 0.651 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.717 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.721 |
LIG_SUMO_SIM_par_1 | 26 | 33 | PF11976 | 0.605 |
LIG_SUMO_SIM_par_1 | 75 | 82 | PF11976 | 0.476 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.658 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.480 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.546 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.614 |
MOD_Cter_Amidation | 102 | 105 | PF01082 | 0.594 |
MOD_GlcNHglycan | 114 | 118 | PF01048 | 0.579 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.639 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.556 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.642 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.685 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.565 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.652 |
MOD_PKA_1 | 131 | 137 | PF00069 | 0.495 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.495 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.546 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.633 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.606 |
MOD_Plk_2-3 | 87 | 93 | PF00069 | 0.635 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.633 |
TRG_DiLeu_BaEn_4 | 64 | 70 | PF01217 | 0.546 |
TRG_ER_diArg_1 | 93 | 96 | PF00400 | 0.491 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P3J1 | Trypanosomatidae | 38% | 100% |
A0A3S7XB75 | Leishmania donovani | 94% | 98% |
A4HPL8 | Leishmania braziliensis | 68% | 100% |
A4ID46 | Leishmania infantum | 94% | 98% |
E9ATD0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |