A very special family of kinetoplastid proteins, carrying multiply amyloid-like segments on their disordered extracellular domain, alongside with RGD motifs. Duplicated in Leishmaniids
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: 4, no: 6 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4HCB1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.784 |
CLV_NRD_NRD_1 | 1 | 3 | PF00675 | 0.781 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.373 |
CLV_PCSK_FUR_1 | 163 | 167 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 1 | 3 | PF00082 | 0.781 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.373 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.431 |
CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.536 |
CLV_PCSK_PC7_1 | 161 | 167 | PF00082 | 0.434 |
CLV_PCSK_PC7_1 | 446 | 452 | PF00082 | 0.452 |
CLV_PCSK_PC7_1 | 45 | 51 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.571 |
DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.371 |
DEG_Nend_UBRbox_1 | 1 | 3 | PF02207 | 0.402 |
DOC_CDC14_PxL_1 | 271 | 279 | PF14671 | 0.625 |
DOC_CYCLIN_RxL_1 | 78 | 91 | PF00134 | 0.716 |
DOC_CYCLIN_yCln2_LP_2 | 59 | 65 | PF00134 | 0.443 |
DOC_MAPK_gen_1 | 159 | 169 | PF00069 | 0.629 |
DOC_MAPK_gen_1 | 49 | 56 | PF00069 | 0.285 |
DOC_MAPK_gen_1 | 80 | 88 | PF00069 | 0.640 |
DOC_MAPK_RevD_3 | 31 | 45 | PF00069 | 0.411 |
DOC_PP2B_LxvP_1 | 241 | 244 | PF13499 | 0.628 |
DOC_PP2B_LxvP_1 | 309 | 312 | PF13499 | 0.664 |
DOC_PP2B_LxvP_1 | 33 | 36 | PF13499 | 0.417 |
DOC_PP2B_LxvP_1 | 377 | 380 | PF13499 | 0.785 |
DOC_PP2B_LxvP_1 | 59 | 62 | PF13499 | 0.443 |
DOC_PP2B_PxIxI_1 | 61 | 67 | PF00149 | 0.251 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.655 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.396 |
LIG_14-3-3_CanoR_1 | 181 | 190 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 450 | 454 | PF00244 | 0.679 |
LIG_BRCT_BRCA1_1 | 280 | 284 | PF00533 | 0.600 |
LIG_BRCT_BRCA1_1 | 5 | 9 | PF00533 | 0.430 |
LIG_CtBP_PxDLS_1 | 30 | 34 | PF00389 | 0.411 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.646 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.768 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.651 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.715 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.349 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.640 |
LIG_Integrin_RGD_1 | 364 | 366 | PF01839 | 0.587 |
LIG_LIR_Gen_1 | 110 | 118 | PF02991 | 0.659 |
LIG_LIR_Gen_1 | 338 | 348 | PF02991 | 0.663 |
LIG_LIR_Gen_1 | 403 | 412 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 110 | 114 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 192 | 197 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 403 | 409 | PF02991 | 0.658 |
LIG_MLH1_MIPbox_1 | 280 | 284 | PF16413 | 0.600 |
LIG_NRP_CendR_1 | 451 | 454 | PF00754 | 0.458 |
LIG_SH2_GRB2like | 283 | 286 | PF00017 | 0.651 |
LIG_SH2_SRC | 437 | 440 | PF00017 | 0.700 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.651 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.700 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.620 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.666 |
LIG_SUMO_SIM_anti_2 | 15 | 23 | PF11976 | 0.532 |
LIG_SUMO_SIM_anti_2 | 268 | 275 | PF11976 | 0.630 |
LIG_SUMO_SIM_par_1 | 15 | 23 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 307 | 313 | PF11976 | 0.662 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.771 |
MOD_CDC14_SPxK_1 | 46 | 49 | PF00782 | 0.354 |
MOD_CDK_SPxK_1 | 43 | 49 | PF00069 | 0.374 |
MOD_CDK_SPxxK_3 | 174 | 181 | PF00069 | 0.622 |
MOD_CDK_SPxxK_3 | 43 | 50 | PF00069 | 0.375 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.614 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.644 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.782 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.774 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.711 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.497 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.821 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.593 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.706 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.462 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.650 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.524 |
MOD_GlcNHglycan | 196 | 200 | PF01048 | 0.491 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.602 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.579 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.479 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.502 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.472 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.618 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.534 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.486 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.610 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.801 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.713 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.522 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.755 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.671 |
MOD_LATS_1 | 362 | 368 | PF00433 | 0.666 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.441 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.437 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.443 |
MOD_N-GLC_1 | 298 | 303 | PF02516 | 0.433 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.465 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.606 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.630 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.648 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.616 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.572 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.671 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.609 |
MOD_NEK2_2 | 449 | 454 | PF00069 | 0.656 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.605 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.733 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.616 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.394 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.662 |
MOD_PKB_1 | 2 | 10 | PF00069 | 0.395 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.609 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.444 |
MOD_Plk_2-3 | 110 | 116 | PF00069 | 0.596 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.761 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.673 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.657 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.664 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.392 |
MOD_SUMO_for_1 | 297 | 300 | PF00179 | 0.625 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.594 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 121 | 124 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 163 | 166 | PF00400 | 0.662 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 75 | 78 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 79 | 82 | PF00400 | 0.612 |
TRG_NLS_MonoExtC_3 | 160 | 165 | PF00514 | 0.631 |
TRG_NLS_MonoExtN_4 | 159 | 166 | PF00514 | 0.633 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVL8 | Leptomonas seymouri | 41% | 93% |
A0A3Q8ILH2 | Leishmania donovani | 63% | 74% |
A0A3S7WX43 | Leishmania donovani | 63% | 74% |
A4HDA2 | Leishmania braziliensis | 99% | 73% |
E9AGZ2 | Leishmania infantum | 62% | 74% |
E9AGZ3 | Leishmania infantum | 63% | 74% |
E9AVQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 76% |
Q4QBR2 | Leishmania major | 63% | 100% |
Q4QBS8 | Leishmania major | 63% | 100% |