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: Q4QCS1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 232 | 236 | PF00656 | 0.483 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 152 | 154 | PF00082 | 0.335 |
DEG_SCF_FBW7_1 | 20 | 26 | PF00400 | 0.548 |
DOC_CKS1_1 | 20 | 25 | PF01111 | 0.564 |
DOC_CKS1_1 | 76 | 81 | PF01111 | 0.669 |
DOC_PIKK_1 | 82 | 90 | PF02985 | 0.549 |
DOC_PP1_RVXF_1 | 184 | 191 | PF00149 | 0.262 |
DOC_SPAK_OSR1_1 | 111 | 115 | PF12202 | 0.625 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.615 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.706 |
LIG_14-3-3_CanoR_1 | 168 | 174 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 186 | 191 | PF00244 | 0.389 |
LIG_BIR_III_2 | 224 | 228 | PF00653 | 0.476 |
LIG_BRCT_BRCA1_1 | 169 | 173 | PF00533 | 0.453 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.584 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.634 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.389 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.483 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.658 |
LIG_LIR_Apic_2 | 117 | 123 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 215 | 219 | PF02991 | 0.463 |
LIG_PCNA_yPIPBox_3 | 136 | 149 | PF02747 | 0.335 |
LIG_PDZ_Class_2 | 231 | 236 | PF00595 | 0.604 |
LIG_SH2_PTP2 | 120 | 123 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 27 | 31 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.521 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.575 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.649 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.699 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.748 |
LIG_SUMO_SIM_anti_2 | 69 | 78 | PF11976 | 0.595 |
LIG_SUMO_SIM_par_1 | 37 | 44 | PF11976 | 0.550 |
LIG_SUMO_SIM_par_1 | 4 | 13 | PF11976 | 0.548 |
LIG_TRAF2_1 | 104 | 107 | PF00917 | 0.494 |
LIG_UBA3_1 | 144 | 152 | PF00899 | 0.335 |
MOD_CDK_SPxK_1 | 75 | 81 | PF00069 | 0.663 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.668 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.625 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.700 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.591 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.630 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.649 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.690 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.291 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.663 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.720 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.617 |
MOD_GlcNHglycan | 62 | 66 | PF01048 | 0.637 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.617 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.584 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.719 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.758 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.546 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.630 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.354 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.699 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.491 |
MOD_NEK2_2 | 175 | 180 | PF00069 | 0.453 |
MOD_NEK2_2 | 218 | 223 | PF00069 | 0.475 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.618 |
MOD_PIKK_1 | 205 | 211 | PF00454 | 0.453 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.453 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.636 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.345 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.546 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.763 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.557 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.614 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.734 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.650 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.670 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.490 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.703 |
TRG_DiLeu_BaEn_2 | 206 | 212 | PF01217 | 0.453 |
TRG_DiLeu_BaEn_4 | 88 | 94 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.453 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IEW9 | Leishmania donovani | 78% | 100% |
A0A3R7K2X3 | Trypanosoma rangeli | 25% | 100% |
A4HYW8 | Leishmania infantum | 78% | 100% |
E9AII0 | Leishmania braziliensis | 47% | 84% |
E9AUR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 89% |