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: A4HDA2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 103 | 107 | PF00656 | 0.421 |
CLV_C14_Caspase3-7 | 535 | 539 | PF00656 | 0.844 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.488 |
CLV_PCSK_FUR_1 | 332 | 336 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 331 | 333 | PF00082 | 0.567 |
CLV_PCSK_PC7_1 | 214 | 220 | PF00082 | 0.590 |
CLV_PCSK_PC7_1 | 330 | 336 | PF00082 | 0.572 |
CLV_PCSK_PC7_1 | 615 | 621 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.634 |
DEG_APCC_DBOX_1 | 218 | 226 | PF00400 | 0.433 |
DEG_APCC_DBOX_1 | 28 | 36 | PF00400 | 0.504 |
DEG_APCC_DBOX_1 | 75 | 83 | PF00400 | 0.429 |
DOC_CDC14_PxL_1 | 440 | 448 | PF14671 | 0.649 |
DOC_CYCLIN_RxL_1 | 247 | 260 | PF00134 | 0.775 |
DOC_CYCLIN_RxL_1 | 29 | 39 | PF00134 | 0.256 |
DOC_CYCLIN_yCln2_LP_2 | 228 | 234 | PF00134 | 0.527 |
DOC_CYCLIN_yCln2_LP_2 | 78 | 84 | PF00134 | 0.548 |
DOC_MAPK_DCC_7 | 76 | 84 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 17 | 26 | PF00069 | 0.587 |
DOC_MAPK_gen_1 | 218 | 225 | PF00069 | 0.322 |
DOC_MAPK_gen_1 | 249 | 257 | PF00069 | 0.756 |
DOC_MAPK_gen_1 | 328 | 338 | PF00069 | 0.748 |
DOC_MAPK_HePTP_8 | 26 | 38 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 29 | 38 | PF00069 | 0.375 |
DOC_MAPK_MEF2A_6 | 76 | 84 | PF00069 | 0.578 |
DOC_MAPK_RevD_3 | 200 | 214 | PF00069 | 0.449 |
DOC_PP2B_LxvP_1 | 202 | 205 | PF13499 | 0.571 |
DOC_PP2B_LxvP_1 | 228 | 231 | PF13499 | 0.527 |
DOC_PP2B_LxvP_1 | 410 | 413 | PF13499 | 0.652 |
DOC_PP2B_LxvP_1 | 478 | 481 | PF13499 | 0.688 |
DOC_PP2B_LxvP_1 | 546 | 549 | PF13499 | 0.846 |
DOC_PP2B_PxIxI_1 | 230 | 236 | PF00149 | 0.278 |
DOC_PP4_FxxP_1 | 84 | 87 | PF00568 | 0.417 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.839 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.834 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.683 |
DOC_USP7_MATH_2 | 172 | 178 | PF00917 | 0.441 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 594 | 599 | PF00397 | 0.688 |
LIG_14-3-3_CanoR_1 | 15 | 20 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 350 | 359 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 619 | 623 | PF00244 | 0.685 |
LIG_BIR_III_4 | 67 | 71 | PF00653 | 0.438 |
LIG_BRCT_BRCA1_1 | 174 | 178 | PF00533 | 0.451 |
LIG_BRCT_BRCA1_1 | 449 | 453 | PF00533 | 0.629 |
LIG_CtBP_PxDLS_1 | 199 | 203 | PF00389 | 0.447 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.397 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.630 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.754 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.761 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.626 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.772 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.420 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.384 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.663 |
LIG_Integrin_RGD_1 | 533 | 535 | PF01839 | 0.658 |
LIG_LIR_Gen_1 | 279 | 287 | PF02991 | 0.800 |
LIG_LIR_Gen_1 | 507 | 517 | PF02991 | 0.766 |
LIG_LIR_Gen_1 | 572 | 581 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 117 | 121 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 279 | 283 | PF02991 | 0.795 |
LIG_LIR_Nem_3 | 314 | 320 | PF02991 | 0.705 |
LIG_LIR_Nem_3 | 361 | 366 | PF02991 | 0.771 |
LIG_LIR_Nem_3 | 507 | 513 | PF02991 | 0.774 |
LIG_LIR_Nem_3 | 572 | 578 | PF02991 | 0.683 |
LIG_MLH1_MIPbox_1 | 449 | 453 | PF16413 | 0.624 |
LIG_NRBOX | 31 | 37 | PF00104 | 0.492 |
LIG_NRP_CendR_1 | 620 | 623 | PF00754 | 0.483 |
LIG_PCNA_yPIPBox_3 | 22 | 35 | PF02747 | 0.538 |
LIG_Rb_pABgroove_1 | 110 | 118 | PF01858 | 0.423 |
LIG_SH2_GRB2like | 452 | 455 | PF00017 | 0.792 |
LIG_SH2_SRC | 606 | 609 | PF00017 | 0.784 |
LIG_SH2_STAP1 | 406 | 410 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.792 |
LIG_SH2_STAT5 | 606 | 609 | PF00017 | 0.784 |
LIG_SH3_2 | 80 | 85 | PF14604 | 0.419 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.653 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.696 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.488 |
LIG_SUMO_SIM_anti_2 | 184 | 192 | PF11976 | 0.603 |
LIG_SUMO_SIM_anti_2 | 437 | 444 | PF11976 | 0.656 |
LIG_SUMO_SIM_par_1 | 184 | 192 | PF11976 | 0.603 |
LIG_SUMO_SIM_par_1 | 33 | 39 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 476 | 482 | PF11976 | 0.686 |
LIG_TRAF2_1 | 377 | 380 | PF00917 | 0.828 |
MOD_CDC14_SPxK_1 | 215 | 218 | PF00782 | 0.391 |
MOD_CDK_SPxK_1 | 212 | 218 | PF00069 | 0.412 |
MOD_CDK_SPxxK_3 | 212 | 219 | PF00069 | 0.416 |
MOD_CDK_SPxxK_3 | 343 | 350 | PF00069 | 0.646 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.616 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.626 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.507 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.500 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.661 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.665 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.832 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.687 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.696 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.456 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.424 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.411 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.837 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.661 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.721 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.815 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.768 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.684 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.441 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.551 |
MOD_GlcNHglycan | 365 | 369 | PF01048 | 0.541 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.256 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.582 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.479 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.608 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.587 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.456 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.608 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.581 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.506 |
MOD_GlcNHglycan | 67 | 71 | PF01048 | 0.762 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.493 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.486 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.630 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.522 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.553 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.534 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.633 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.792 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.522 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.839 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.735 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.709 |
MOD_LATS_1 | 531 | 537 | PF00433 | 0.702 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.603 |
MOD_N-GLC_1 | 295 | 300 | PF02516 | 0.478 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.464 |
MOD_N-GLC_1 | 453 | 458 | PF02516 | 0.582 |
MOD_N-GLC_1 | 467 | 472 | PF02516 | 0.468 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.513 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.529 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.802 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.644 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.656 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.407 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.496 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.759 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.648 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.594 |
MOD_NEK2_2 | 295 | 300 | PF00069 | 0.636 |
MOD_NEK2_2 | 618 | 623 | PF00069 | 0.682 |
MOD_PIKK_1 | 447 | 453 | PF00454 | 0.628 |
MOD_PIKK_1 | 485 | 491 | PF00454 | 0.772 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.721 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.652 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.435 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.498 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.445 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.432 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.654 |
MOD_Plk_2-3 | 279 | 285 | PF00069 | 0.621 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.448 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.398 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.823 |
MOD_Plk_4 | 602 | 608 | PF00069 | 0.696 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.442 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.428 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.686 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.540 |
MOD_ProDKin_1 | 594 | 600 | PF00069 | 0.689 |
MOD_SUMO_for_1 | 466 | 469 | PF00179 | 0.646 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.620 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 244 | 247 | PF00400 | 0.717 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.699 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 332 | 335 | PF00400 | 0.776 |
TRG_ER_diArg_1 | 618 | 620 | PF00400 | 0.685 |
TRG_NLS_MonoExtC_3 | 329 | 334 | PF00514 | 0.769 |
TRG_NLS_MonoExtN_4 | 328 | 335 | PF00514 | 0.770 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ILH2 | Leishmania donovani | 57% | 100% |
A0A3S7WX43 | Leishmania donovani | 57% | 100% |
A4HCB1 | Leishmania braziliensis | 99% | 100% |
E9AGZ2 | Leishmania infantum | 58% | 100% |
E9AGZ3 | Leishmania infantum | 58% | 100% |
E9AVQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |
Q4QBR2 | Leishmania major | 57% | 100% |
Q4QBS8 | Leishmania major | 57% | 100% |