Although predicted to have a multi-helical architecture, the protein is not hydrophobic enough for a membrane protein.. Unique to kinetoplastids, fast-evolving and duplicated multiple times.
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: 2 |
NetGPI | no | yes: 0, no: 2 |
Related structures:
AlphaFold database: A4HJ75
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.451 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.665 |
DEG_APCC_DBOX_1 | 15 | 23 | PF00400 | 0.432 |
DOC_CKS1_1 | 138 | 143 | PF01111 | 0.504 |
DOC_CKS1_1 | 253 | 258 | PF01111 | 0.456 |
DOC_CYCLIN_RxL_1 | 108 | 117 | PF00134 | 0.424 |
DOC_MAPK_gen_1 | 217 | 227 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 89 | 96 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 220 | 229 | PF00069 | 0.453 |
DOC_PP1_RVXF_1 | 258 | 265 | PF00149 | 0.443 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.527 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.453 |
LIG_14-3-3_CanoR_1 | 220 | 229 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 23 | 29 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 52 | 57 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 78 | 84 | PF00244 | 0.690 |
LIG_14-3-3_CterR_2 | 319 | 321 | PF00244 | 0.487 |
LIG_Actin_WH2_2 | 255 | 273 | PF00022 | 0.460 |
LIG_eIF4E_1 | 199 | 205 | PF01652 | 0.482 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.406 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.508 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.461 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.492 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.471 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.511 |
LIG_Integrin_RGD_1 | 293 | 295 | PF01839 | 0.491 |
LIG_Integrin_RGD_1 | 40 | 42 | PF01839 | 0.478 |
LIG_LIR_Apic_2 | 250 | 256 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.601 |
LIG_PCNA_yPIPBox_3 | 111 | 119 | PF02747 | 0.465 |
LIG_REV1ctd_RIR_1 | 261 | 270 | PF16727 | 0.451 |
LIG_SH2_CRK | 110 | 114 | PF00017 | 0.481 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.455 |
LIG_SH2_GRB2like | 119 | 122 | PF00017 | 0.483 |
LIG_SH2_STAT3 | 157 | 160 | PF00017 | 0.454 |
LIG_SH2_STAT3 | 199 | 202 | PF00017 | 0.480 |
LIG_SH2_STAT3 | 83 | 86 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.734 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.718 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.594 |
LIG_UBA3_1 | 225 | 234 | PF00899 | 0.444 |
LIG_UBA3_1 | 28 | 36 | PF00899 | 0.704 |
MOD_CDK_SPK_2 | 137 | 142 | PF00069 | 0.501 |
MOD_CDK_SPK_2 | 205 | 210 | PF00069 | 0.490 |
MOD_CDK_SPxK_1 | 252 | 258 | PF00069 | 0.454 |
MOD_CDK_SPxxK_3 | 137 | 144 | PF00069 | 0.506 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.711 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.526 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.630 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.440 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.507 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.487 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.484 |
MOD_GlcNHglycan | 184 | 188 | PF01048 | 0.482 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.462 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.609 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.472 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.407 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.534 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.777 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.701 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.641 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.526 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.506 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.714 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.467 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.489 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.589 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.526 |
MOD_NEK2_2 | 18 | 23 | PF00069 | 0.430 |
MOD_PIKK_1 | 236 | 242 | PF00454 | 0.440 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.514 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.412 |
MOD_PKB_1 | 218 | 226 | PF00069 | 0.458 |
MOD_Plk_2-3 | 42 | 48 | PF00069 | 0.506 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.406 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.423 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.462 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.450 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.542 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.670 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.503 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.531 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.728 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.454 |
MOD_SUMO_rev_2 | 267 | 272 | PF00179 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 217 | 222 | PF01217 | 0.712 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.470 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
E8NHD2 | Leishmania infantum | 27% | 70% |