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: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 17 |
NetGPI | no | yes: 0, no: 17 |
Related structures:
AlphaFold database: A4HJW7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.744 |
CLV_NRD_NRD_1 | 407 | 409 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.545 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 354 | 356 | PF00082 | 0.730 |
CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.510 |
CLV_PCSK_PC7_1 | 135 | 141 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.717 |
DEG_SCF_FBW7_1 | 218 | 224 | PF00400 | 0.502 |
DOC_CKS1_1 | 218 | 223 | PF01111 | 0.503 |
DOC_CKS1_1 | 35 | 40 | PF01111 | 0.380 |
DOC_CYCLIN_RxL_1 | 22 | 36 | PF00134 | 0.394 |
DOC_CYCLIN_RxL_1 | 61 | 71 | PF00134 | 0.554 |
DOC_CYCLIN_yCln2_LP_2 | 396 | 402 | PF00134 | 0.306 |
DOC_MAPK_gen_1 | 22 | 32 | PF00069 | 0.407 |
DOC_MAPK_gen_1 | 62 | 68 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 383 | 390 | PF00069 | 0.648 |
DOC_MAPK_RevD_3 | 395 | 409 | PF00069 | 0.341 |
DOC_PP1_RVXF_1 | 26 | 33 | PF00149 | 0.392 |
DOC_PP2B_LxvP_1 | 396 | 399 | PF13499 | 0.383 |
DOC_PP4_FxxP_1 | 308 | 311 | PF00568 | 0.508 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.628 |
DOC_USP7_MATH_2 | 164 | 170 | PF00917 | 0.712 |
DOC_USP7_UBL2_3 | 361 | 365 | PF12436 | 0.491 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.384 |
LIG_14-3-3_CanoR_1 | 111 | 115 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 135 | 142 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 199 | 205 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 236 | 240 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 257 | 261 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 283 | 287 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 371 | 379 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 95 | 100 | PF00244 | 0.701 |
LIG_Actin_WH2_2 | 267 | 285 | PF00022 | 0.700 |
LIG_BRCT_BRCA1_1 | 97 | 101 | PF00533 | 0.663 |
LIG_CSL_BTD_1 | 218 | 221 | PF09270 | 0.753 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.599 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.544 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.690 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.729 |
LIG_LIR_Apic_2 | 306 | 311 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 37 | 44 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 418 | 426 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 435 | 445 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 70 | 80 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 418 | 423 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.428 |
LIG_MLH1_MIPbox_1 | 97 | 101 | PF16413 | 0.416 |
LIG_PCNA_yPIPBox_3 | 14 | 28 | PF02747 | 0.433 |
LIG_SH2_CRK | 121 | 125 | PF00017 | 0.508 |
LIG_SH2_PTP2 | 420 | 423 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.670 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.707 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.553 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.484 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.756 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.700 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.824 |
LIG_SUMO_SIM_anti_2 | 268 | 275 | PF11976 | 0.719 |
LIG_SUMO_SIM_anti_2 | 8 | 16 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 200 | 207 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 228 | 234 | PF11976 | 0.487 |
LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.613 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.498 |
LIG_TYR_ITIM | 119 | 124 | PF00017 | 0.439 |
LIG_UBA3_1 | 125 | 133 | PF00899 | 0.365 |
LIG_UBA3_1 | 401 | 409 | PF00899 | 0.442 |
LIG_UBA3_1 | 440 | 447 | PF00899 | 0.553 |
MOD_CDK_SPK_2 | 34 | 39 | PF00069 | 0.384 |
MOD_CDK_SPxxK_3 | 250 | 257 | PF00069 | 0.740 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.428 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.557 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.441 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.628 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.706 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.532 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.764 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.613 |
MOD_GlcNHglycan | 321 | 325 | PF01048 | 0.787 |
MOD_GlcNHglycan | 347 | 351 | PF01048 | 0.761 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.578 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.815 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.776 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.544 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.580 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.684 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.600 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.708 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.554 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.556 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.488 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.744 |
MOD_N-GLC_1 | 377 | 382 | PF02516 | 0.464 |
MOD_N-GLC_2 | 120 | 122 | PF02516 | 0.534 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.604 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.468 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.712 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.764 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.468 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.690 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.682 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.529 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.625 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.640 |
MOD_PIKK_1 | 219 | 225 | PF00454 | 0.656 |
MOD_PKA_1 | 408 | 414 | PF00069 | 0.573 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.351 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.478 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.692 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.573 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.462 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.609 |
MOD_PKB_1 | 318 | 326 | PF00069 | 0.541 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.670 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.396 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.377 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.501 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.411 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.559 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.696 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.500 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.750 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.741 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.380 |
MOD_SUMO_for_1 | 353 | 356 | PF00179 | 0.480 |
TRG_DiLeu_BaEn_1 | 392 | 397 | PF01217 | 0.349 |
TRG_DiLeu_BaLyEn_6 | 225 | 230 | PF01217 | 0.730 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.580 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.553 |
TRG_ER_diArg_1 | 139 | 141 | PF00400 | 0.431 |
TRG_NLS_Bipartite_1 | 354 | 373 | PF00514 | 0.714 |
TRG_Pf-PMV_PEXEL_1 | 178 | 183 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 447 | 451 | PF00026 | 0.508 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IFG5 | Leishmania donovani | 59% | 73% |
A0A3Q8ISI8 | Leishmania donovani | 60% | 73% |
A0A3S7X4A3 | Leishmania donovani | 59% | 73% |
A4HJ70 | Leishmania braziliensis | 92% | 100% |
A4HJ71 | Leishmania braziliensis | 87% | 100% |
A4I6I2 | Leishmania infantum | 59% | 68% |
A4I6L8 | Leishmania infantum | 60% | 73% |
E8NHD1 | Leishmania infantum | 60% | 76% |
E8NHD2 | Leishmania infantum | 60% | 98% |
E8NHE7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 73% |
E8NHE8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 73% |
E9B1P3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 73% |
Q4Q6G7 | Leishmania major | 60% | 100% |
Q4Q6G8 | Leishmania major | 61% | 100% |
Q4Q6H0 | Leishmania major | 60% | 100% |
Q9BHE5 | Leishmania major | 61% | 100% |