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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4H858
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 116 | 120 | PF00656 | 0.544 |
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.603 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.482 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.561 |
DEG_APCC_DBOX_1 | 97 | 105 | PF00400 | 0.424 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.561 |
DEG_SPOP_SBC_1 | 172 | 176 | PF00917 | 0.628 |
DOC_CKS1_1 | 185 | 190 | PF01111 | 0.524 |
DOC_CKS1_1 | 263 | 268 | PF01111 | 0.551 |
DOC_MAPK_MEF2A_6 | 29 | 38 | PF00069 | 0.502 |
DOC_PP2B_LxvP_1 | 260 | 263 | PF13499 | 0.551 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.667 |
DOC_USP7_MATH_2 | 211 | 217 | PF00917 | 0.605 |
DOC_USP7_UBL2_3 | 197 | 201 | PF12436 | 0.612 |
DOC_USP7_UBL2_3 | 242 | 246 | PF12436 | 0.607 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.555 |
LIG_14-3-3_CanoR_1 | 258 | 263 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 29 | 38 | PF00244 | 0.598 |
LIG_Actin_RPEL_3 | 34 | 53 | PF02755 | 0.387 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.502 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.564 |
LIG_Integrin_RGD_1 | 113 | 115 | PF01839 | 0.517 |
LIG_LIR_Gen_1 | 24 | 35 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 290 | 301 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.515 |
LIG_NRP_CendR_1 | 311 | 314 | PF00754 | 0.605 |
LIG_SH2_PTP2 | 27 | 30 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.502 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.691 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.666 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.642 |
LIG_TRAF2_1 | 22 | 25 | PF00917 | 0.519 |
LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.694 |
LIG_UBA3_1 | 94 | 102 | PF00899 | 0.413 |
LIG_WW_2 | 236 | 239 | PF00397 | 0.522 |
MOD_CDK_SPxK_1 | 184 | 190 | PF00069 | 0.529 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.632 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.707 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.571 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.754 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.636 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.589 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.544 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.544 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.579 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.698 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.782 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.570 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.695 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.688 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.607 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.679 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.638 |
MOD_GlcNHglycan | 42 | 46 | PF01048 | 0.485 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.590 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.510 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.620 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.764 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.583 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.606 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.690 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.592 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.734 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.600 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.671 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.551 |
MOD_N-GLC_1 | 223 | 228 | PF02516 | 0.555 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.702 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.553 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.548 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.583 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.505 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.725 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.552 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.701 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.457 |
MOD_Plk_2-3 | 139 | 145 | PF00069 | 0.566 |
MOD_Plk_2-3 | 146 | 152 | PF00069 | 0.671 |
MOD_Plk_2-3 | 281 | 287 | PF00069 | 0.457 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.579 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.578 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.707 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.745 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.768 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.476 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.559 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.553 |
TRG_DiLeu_BaEn_4 | 255 | 261 | PF01217 | 0.560 |
TRG_DiLeu_BaLyEn_6 | 187 | 192 | PF01217 | 0.645 |
TRG_DiLeu_BaLyEn_6 | 268 | 273 | PF01217 | 0.553 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 190 | 194 | PF00026 | 0.687 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WTH2 | Leishmania donovani | 58% | 97% |
A4HWI4 | Leishmania infantum | 57% | 97% |
E9AQ85 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 99% |
Q4QF98 | Leishmania major | 63% | 100% |