Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 6 |
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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3Q8ICK8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.556 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 148 | 150 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.561 |
DEG_APCC_DBOX_1 | 148 | 156 | PF00400 | 0.375 |
DEG_APCC_DBOX_1 | 28 | 36 | PF00400 | 0.415 |
DOC_MAPK_gen_1 | 191 | 200 | PF00069 | 0.565 |
DOC_MAPK_gen_1 | 203 | 211 | PF00069 | 0.340 |
DOC_MAPK_MEF2A_6 | 179 | 186 | PF00069 | 0.506 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.578 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.485 |
DOC_USP7_UBL2_3 | 125 | 129 | PF12436 | 0.420 |
DOC_USP7_UBL2_3 | 133 | 137 | PF12436 | 0.421 |
DOC_USP7_UBL2_3 | 144 | 148 | PF12436 | 0.501 |
DOC_USP7_UBL2_3 | 158 | 162 | PF12436 | 0.441 |
DOC_USP7_UBL2_3 | 171 | 175 | PF12436 | 0.384 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.714 |
LIG_14-3-3_CanoR_1 | 203 | 209 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 213 | 223 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 67 | 73 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 92 | 99 | PF00244 | 0.679 |
LIG_Actin_WH2_2 | 110 | 127 | PF00022 | 0.468 |
LIG_APCC_Cbox_2 | 73 | 79 | PF00515 | 0.551 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.589 |
LIG_Dynein_DLC8_1 | 201 | 207 | PF01221 | 0.348 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.464 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.498 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.540 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.558 |
LIG_LIR_Gen_1 | 196 | 201 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 220 | 230 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 196 | 200 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.463 |
LIG_SH2_NCK_1 | 24 | 28 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 172 | 176 | PF00017 | 0.498 |
LIG_SH2_STAP1 | 24 | 28 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.392 |
LIG_SUMO_SIM_par_1 | 59 | 66 | PF11976 | 0.417 |
LIG_UBA3_1 | 127 | 133 | PF00899 | 0.419 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.527 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.526 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.468 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.548 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.628 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.428 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.499 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.452 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.545 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.680 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.728 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.658 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.489 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.458 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.484 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.654 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.765 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.585 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.630 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.478 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.559 |
MOD_PKA_1 | 147 | 153 | PF00069 | 0.505 |
MOD_PKA_1 | 15 | 21 | PF00069 | 0.462 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.595 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.464 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.630 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.482 |
MOD_Plk_2-3 | 151 | 157 | PF00069 | 0.459 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.413 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.698 |
MOD_SUMO_rev_2 | 118 | 127 | PF00179 | 0.490 |
MOD_SUMO_rev_2 | 150 | 160 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 4 | 13 | PF00179 | 0.626 |
TRG_DiLeu_BaEn_1 | 196 | 201 | PF01217 | 0.463 |
TRG_DiLeu_BaEn_1 | 9 | 14 | PF01217 | 0.538 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 191 | 196 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCG3 | Leptomonas seymouri | 47% | 99% |
A0A1X0NYD1 | Trypanosomatidae | 28% | 90% |
A0A3R7KGK2 | Trypanosoma rangeli | 26% | 100% |
A4HCW9 | Leishmania braziliensis | 59% | 100% |
A4I0E9 | Leishmania infantum | 100% | 100% |
E9AWB2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4QB63 | Leishmania major | 90% | 100% |