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: A0A3Q8IQI1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.357 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.380 |
CLV_PCSK_PC1ET2_1 | 188 | 190 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.376 |
DEG_APCC_DBOX_1 | 146 | 154 | PF00400 | 0.706 |
DEG_APCC_DBOX_1 | 162 | 170 | PF00400 | 0.598 |
DOC_CKS1_1 | 68 | 73 | PF01111 | 0.544 |
DOC_CYCLIN_RxL_1 | 188 | 201 | PF00134 | 0.376 |
DOC_MAPK_gen_1 | 161 | 169 | PF00069 | 0.602 |
DOC_MAPK_gen_1 | 188 | 198 | PF00069 | 0.372 |
DOC_PP4_FxxP_1 | 68 | 71 | PF00568 | 0.683 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.584 |
DOC_USP7_UBL2_3 | 113 | 117 | PF12436 | 0.672 |
DOC_USP7_UBL2_3 | 157 | 161 | PF12436 | 0.640 |
DOC_USP7_UBL2_3 | 188 | 192 | PF12436 | 0.430 |
DOC_USP7_UBL2_3 | 216 | 220 | PF12436 | 0.376 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.641 |
LIG_14-3-3_CanoR_1 | 147 | 151 | PF00244 | 0.651 |
LIG_APCC_ABBA_1 | 196 | 201 | PF00400 | 0.376 |
LIG_EVH1_2 | 37 | 41 | PF00568 | 0.546 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.605 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.671 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.734 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.430 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.346 |
LIG_LIR_Apic_2 | 66 | 71 | PF02991 | 0.709 |
LIG_LIR_Gen_1 | 17 | 28 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.669 |
LIG_Pex14_2 | 126 | 130 | PF04695 | 0.544 |
LIG_PTB_Apo_2 | 62 | 69 | PF02174 | 0.660 |
LIG_Rb_pABgroove_1 | 103 | 111 | PF01858 | 0.745 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.376 |
LIG_SH2_CRK | 82 | 86 | PF00017 | 0.723 |
LIG_SH2_NCK_1 | 120 | 124 | PF00017 | 0.675 |
LIG_SH2_SRC | 93 | 96 | PF00017 | 0.617 |
LIG_SH2_STAP1 | 234 | 238 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.684 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.622 |
LIG_SH3_4 | 113 | 120 | PF00018 | 0.710 |
LIG_TRAF2_1 | 182 | 185 | PF00917 | 0.430 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.346 |
LIG_UBA3_1 | 108 | 116 | PF00899 | 0.668 |
LIG_UBA3_1 | 214 | 220 | PF00899 | 0.376 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.655 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.671 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.643 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.746 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.604 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.656 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.721 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.430 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.346 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.392 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.668 |
MOD_Cter_Amidation | 133 | 136 | PF01082 | 0.714 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.673 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.703 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.658 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.564 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.682 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.614 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.500 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.634 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.691 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.544 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.614 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.597 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.638 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.668 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.693 |
MOD_N-GLC_1 | 23 | 28 | PF02516 | 0.486 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.689 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.759 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.606 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.609 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.662 |
MOD_PIKK_1 | 205 | 211 | PF00454 | 0.315 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.753 |
MOD_PK_1 | 81 | 87 | PF00069 | 0.646 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.684 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.588 |
MOD_Plk_2-3 | 146 | 152 | PF00069 | 0.658 |
MOD_Plk_2-3 | 223 | 229 | PF00069 | 0.430 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.613 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.625 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.616 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.707 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.639 |
MOD_SUMO_rev_2 | 145 | 150 | PF00179 | 0.759 |
MOD_SUMO_rev_2 | 158 | 162 | PF00179 | 0.585 |
MOD_SUMO_rev_2 | 183 | 190 | PF00179 | 0.501 |
TRG_DiLeu_BaLyEn_6 | 162 | 167 | PF01217 | 0.598 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.652 |
TRG_ER_diArg_1 | 162 | 165 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 231 | 233 | PF00400 | 0.501 |
TRG_NLS_MonoExtN_4 | 189 | 196 | PF00514 | 0.353 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7W1 | Leptomonas seymouri | 58% | 85% |
A0A0S4J306 | Bodo saltans | 36% | 100% |
A4HNS1 | Leishmania braziliensis | 73% | 100% |
A4ICS3 | Leishmania infantum | 100% | 100% |
E9ASI1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q215 | Leishmania major | 92% | 100% |