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: A0A3Q8IEW9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.376 |
CLV_PCSK_PC1ET2_1 | 152 | 154 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.589 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.586 |
DOC_CKS1_1 | 76 | 81 | PF01111 | 0.718 |
DOC_CYCLIN_yCln2_LP_2 | 20 | 26 | PF00134 | 0.582 |
DOC_PP2B_LxvP_1 | 20 | 23 | PF13499 | 0.582 |
DOC_SPAK_OSR1_1 | 111 | 115 | PF12202 | 0.656 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.800 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.376 |
DOC_USP7_MATH_2 | 204 | 210 | PF00917 | 0.326 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.727 |
LIG_14-3-3_CanoR_1 | 168 | 174 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 186 | 191 | PF00244 | 0.430 |
LIG_BIR_III_2 | 223 | 227 | PF00653 | 0.485 |
LIG_BRCT_BRCA1_1 | 169 | 173 | PF00533 | 0.501 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.402 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.412 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.638 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.390 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.613 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.653 |
LIG_HCF-1_HBM_1 | 132 | 135 | PF13415 | 0.326 |
LIG_LIR_Apic_2 | 117 | 123 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.430 |
LIG_PCNA_yPIPBox_3 | 136 | 149 | PF02747 | 0.376 |
LIG_PDZ_Class_2 | 230 | 235 | PF00595 | 0.633 |
LIG_SH2_PTP2 | 120 | 123 | PF00017 | 0.557 |
LIG_SH2_STAP1 | 165 | 169 | PF00017 | 0.287 |
LIG_SH2_STAT3 | 34 | 37 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.450 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.611 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.614 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.750 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.767 |
LIG_SUMO_SIM_par_1 | 89 | 95 | PF11976 | 0.560 |
LIG_UBA3_1 | 144 | 152 | PF00899 | 0.376 |
MOD_CDK_SPK_2 | 38 | 43 | PF00069 | 0.596 |
MOD_CDK_SPxK_1 | 75 | 81 | PF00069 | 0.703 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.287 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.733 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.734 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.646 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.326 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.823 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.690 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.800 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.736 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.771 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.633 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.677 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.355 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.371 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.665 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.786 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.739 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.608 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.376 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.743 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.482 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.316 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.404 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.611 |
MOD_NEK2_2 | 175 | 180 | PF00069 | 0.501 |
MOD_NEK2_2 | 217 | 222 | PF00069 | 0.430 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.653 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.501 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.436 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.350 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.430 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.825 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.359 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.735 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.631 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.502 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.596 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.634 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.726 |
TRG_DiLeu_BaEn_2 | 205 | 211 | PF01217 | 0.430 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.430 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I766 | Leptomonas seymouri | 44% | 69% |
A0A3R7K2X3 | Trypanosoma rangeli | 30% | 100% |
A4HYW8 | Leishmania infantum | 99% | 100% |
E9AII0 | Leishmania braziliensis | 48% | 100% |
E9AUR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4QCS1 | Leishmania major | 78% | 100% |