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: 5 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: E9AVQ1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.408 |
CLV_C14_Caspase3-7 | 353 | 357 | PF00656 | 0.636 |
CLV_C14_Caspase3-7 | 539 | 543 | PF00656 | 0.850 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.522 |
CLV_PCSK_FUR_1 | 250 | 254 | PF00082 | 0.497 |
CLV_PCSK_FUR_1 | 335 | 339 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.768 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 252 | 254 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 334 | 336 | PF00082 | 0.577 |
CLV_PCSK_PC7_1 | 248 | 254 | PF00082 | 0.487 |
CLV_PCSK_PC7_1 | 333 | 339 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.543 |
DEG_APCC_DBOX_1 | 221 | 229 | PF00400 | 0.433 |
DEG_COP1_1 | 121 | 131 | PF00400 | 0.430 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.770 |
DOC_CYCLIN_RxL_1 | 250 | 263 | PF00134 | 0.781 |
DOC_CYCLIN_RxL_1 | 459 | 469 | PF00134 | 0.670 |
DOC_CYCLIN_yCln2_LP_2 | 231 | 237 | PF00134 | 0.527 |
DOC_CYCLIN_yCln2_LP_2 | 80 | 86 | PF00134 | 0.606 |
DOC_MAPK_gen_1 | 250 | 260 | PF00069 | 0.769 |
DOC_MAPK_gen_1 | 300 | 307 | PF00069 | 0.683 |
DOC_MAPK_MEF2A_6 | 21 | 30 | PF00069 | 0.591 |
DOC_MAPK_MEF2A_6 | 69 | 78 | PF00069 | 0.603 |
DOC_PP1_RVXF_1 | 19 | 26 | PF00149 | 0.519 |
DOC_PP2B_LxvP_1 | 231 | 234 | PF13499 | 0.527 |
DOC_PP2B_LxvP_1 | 71 | 74 | PF13499 | 0.566 |
DOC_SPAK_OSR1_1 | 302 | 306 | PF12202 | 0.772 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.859 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.836 |
DOC_USP7_UBL2_3 | 252 | 256 | PF12436 | 0.718 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.633 |
LIG_14-3-3_CanoR_1 | 143 | 151 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 16 | 25 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 167 | 175 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 176 | 182 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 496 | 503 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 569 | 576 | PF00244 | 0.813 |
LIG_APCC_ABBAyCdc20_2 | 593 | 599 | PF00400 | 0.633 |
LIG_CaM_NSCaTE_8 | 177 | 184 | PF13499 | 0.417 |
LIG_Clathr_ClatBox_1 | 117 | 121 | PF01394 | 0.491 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.598 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.864 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.800 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.776 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.576 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.767 |
LIG_Integrin_isoDGR_2 | 141 | 143 | PF01839 | 0.748 |
LIG_Integrin_RGD_1 | 367 | 369 | PF01839 | 0.444 |
LIG_Integrin_RGD_1 | 537 | 539 | PF01839 | 0.667 |
LIG_LIR_Gen_1 | 108 | 119 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 282 | 291 | PF02991 | 0.820 |
LIG_LIR_Gen_1 | 301 | 311 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 35 | 43 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 515 | 525 | PF02991 | 0.790 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 282 | 286 | PF02991 | 0.814 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.730 |
LIG_LIR_Nem_3 | 515 | 520 | PF02991 | 0.786 |
LIG_NRBOX | 28 | 34 | PF00104 | 0.501 |
LIG_SH2_GRB2like | 456 | 459 | PF00017 | 0.816 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.703 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.715 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.435 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.455 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.641 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.633 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.831 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.789 |
LIG_SH3_3 | 553 | 559 | PF00018 | 0.679 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.598 |
LIG_SUMO_SIM_anti_2 | 186 | 196 | PF11976 | 0.638 |
LIG_SUMO_SIM_anti_2 | 221 | 227 | PF11976 | 0.223 |
LIG_SUMO_SIM_anti_2 | 77 | 82 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 186 | 196 | PF11976 | 0.623 |
LIG_SUMO_SIM_par_1 | 29 | 35 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 74 | 79 | PF11976 | 0.480 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.575 |
LIG_TRAF2_1 | 380 | 383 | PF00917 | 0.850 |
LIG_WRC_WIRS_1 | 33 | 38 | PF05994 | 0.448 |
LIG_WRC_WIRS_1 | 520 | 525 | PF05994 | 0.749 |
MOD_CDC14_SPxK_1 | 364 | 367 | PF00782 | 0.641 |
MOD_CDK_SPK_2 | 11 | 16 | PF00069 | 0.702 |
MOD_CDK_SPxK_1 | 287 | 293 | PF00069 | 0.708 |
MOD_CDK_SPxK_1 | 361 | 367 | PF00069 | 0.643 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.630 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.633 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.520 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.484 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.846 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.641 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.403 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.855 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.818 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.669 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.830 |
MOD_DYRK1A_RPxSP_1 | 11 | 15 | PF00069 | 0.615 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.816 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.793 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.698 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.662 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.636 |
MOD_GlcNHglycan | 404 | 408 | PF01048 | 0.541 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.623 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.566 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.645 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.485 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.461 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.636 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.618 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.785 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.778 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.499 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.754 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.570 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.481 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.488 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.547 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.458 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.719 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.805 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.775 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.850 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.705 |
MOD_LATS_1 | 535 | 541 | PF00433 | 0.709 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.608 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.518 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.592 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.808 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.504 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.772 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.668 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.491 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.620 |
MOD_NEK2_2 | 491 | 496 | PF00069 | 0.776 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.776 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.541 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.652 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.585 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.505 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.727 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.771 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.702 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.654 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.813 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.756 |
MOD_Plk_2-3 | 568 | 574 | PF00069 | 0.813 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.860 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.698 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.490 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.762 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.540 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.450 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.479 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.708 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.810 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.634 |
TRG_DiLeu_BaEn_1 | 459 | 464 | PF01217 | 0.589 |
TRG_DiLeu_LyEn_5 | 459 | 464 | PF01217 | 0.591 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 247 | 250 | PF00400 | 0.724 |
TRG_ER_diArg_1 | 300 | 303 | PF00400 | 0.720 |
TRG_ER_diArg_1 | 335 | 338 | PF00400 | 0.783 |
TRG_NLS_MonoExtC_3 | 251 | 256 | PF00514 | 0.711 |
TRG_NLS_MonoExtC_3 | 332 | 337 | PF00514 | 0.781 |
TRG_NLS_MonoExtN_4 | 250 | 257 | PF00514 | 0.711 |
TRG_NLS_MonoExtN_4 | 331 | 338 | PF00514 | 0.782 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ILH2 | Leishmania donovani | 82% | 97% |
A0A3S7WX43 | Leishmania donovani | 82% | 97% |
A4HCB1 | Leishmania braziliensis | 62% | 100% |
A4HDA2 | Leishmania braziliensis | 56% | 100% |
E9AGZ2 | Leishmania infantum | 82% | 97% |
E9AGZ3 | Leishmania infantum | 82% | 97% |
Q4QBR2 | Leishmania major | 83% | 100% |
Q4QBS8 | Leishmania major | 83% | 100% |