An absolutely unique fold restricted to kinetoplastids. most predictions are too weak to assume any secure topology.
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 | yes | yes: 2, no: 5 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9AW53
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 226 | 230 | PF00656 | 0.472 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.540 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.415 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.570 |
DEG_ODPH_VHL_1 | 76 | 89 | PF01847 | 0.351 |
DOC_CYCLIN_yCln2_LP_2 | 205 | 211 | PF00134 | 0.596 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.567 |
DOC_MAPK_NFAT4_5 | 2 | 10 | PF00069 | 0.567 |
DOC_MAPK_RevD_3 | 245 | 261 | PF00069 | 0.369 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.546 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.701 |
LIG_14-3-3_CanoR_1 | 149 | 159 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 49 | 58 | PF00244 | 0.484 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.381 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.460 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.385 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.357 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.534 |
LIG_LIR_Gen_1 | 213 | 224 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 238 | 248 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.456 |
LIG_MAD2 | 64 | 72 | PF02301 | 0.433 |
LIG_MYND_1 | 207 | 211 | PF01753 | 0.380 |
LIG_Pex14_1 | 223 | 227 | PF04695 | 0.596 |
LIG_RPA_C_Fungi | 46 | 58 | PF08784 | 0.576 |
LIG_SH2_CRK | 216 | 220 | PF00017 | 0.201 |
LIG_SH2_SRC | 188 | 191 | PF00017 | 0.223 |
LIG_SH2_STAP1 | 216 | 220 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.320 |
LIG_SH3_1 | 64 | 70 | PF00018 | 0.515 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.491 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.381 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.663 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.459 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.617 |
LIG_Sin3_3 | 158 | 165 | PF02671 | 0.297 |
LIG_SUMO_SIM_anti_2 | 127 | 132 | PF11976 | 0.380 |
LIG_SUMO_SIM_anti_2 | 3 | 9 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 12 | 17 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 158 | 164 | PF11976 | 0.361 |
LIG_TYR_ITIM | 178 | 183 | PF00017 | 0.543 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.729 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.637 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.652 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.380 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.582 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.573 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.616 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.558 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.380 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.558 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.475 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.546 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.380 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.290 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.401 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.398 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.598 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.458 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.555 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.493 |
MOD_Plk_2-3 | 273 | 279 | PF00069 | 0.639 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.458 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.383 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.381 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.444 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.633 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.552 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.380 |
TRG_NLS_MonoExtN_4 | 140 | 147 | PF00514 | 0.539 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P307 | Leptomonas seymouri | 60% | 100% |
A0A3Q8ICG4 | Leishmania donovani | 93% | 100% |
A4HCR4 | Leishmania braziliensis | 81% | 100% |
A4I089 | Leishmania infantum | 93% | 100% |
C9ZV06 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
Q4QBC4 | Leishmania major | 92% | 100% |