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: Q4QBS8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 539 | 543 | PF00656 | 0.780 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.472 |
CLV_PCSK_FUR_1 | 250 | 254 | PF00082 | 0.435 |
CLV_PCSK_FUR_1 | 335 | 339 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 252 | 254 | PF00082 | 0.445 |
CLV_PCSK_PC1ET2_1 | 334 | 336 | PF00082 | 0.507 |
CLV_PCSK_PC7_1 | 248 | 254 | PF00082 | 0.427 |
CLV_PCSK_PC7_1 | 333 | 339 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.481 |
DEG_APCC_DBOX_1 | 221 | 229 | PF00400 | 0.364 |
DEG_APCC_DBOX_1 | 24 | 32 | PF00400 | 0.473 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.716 |
DEG_SPOP_SBC_1 | 128 | 132 | PF00917 | 0.546 |
DEG_SPOP_SBC_1 | 155 | 159 | PF00917 | 0.516 |
DEG_SPOP_SBC_1 | 202 | 206 | PF00917 | 0.520 |
DEG_SPOP_SBC_1 | 438 | 442 | PF00917 | 0.774 |
DOC_CKS1_1 | 43 | 48 | PF01111 | 0.500 |
DOC_CYCLIN_RxL_1 | 250 | 263 | PF00134 | 0.710 |
DOC_CYCLIN_yCln2_LP_2 | 231 | 237 | PF00134 | 0.430 |
DOC_CYCLIN_yCln2_LP_2 | 80 | 86 | PF00134 | 0.541 |
DOC_MAPK_gen_1 | 250 | 260 | PF00069 | 0.760 |
DOC_MAPK_gen_1 | 300 | 307 | PF00069 | 0.653 |
DOC_MAPK_gen_1 | 331 | 341 | PF00069 | 0.736 |
DOC_MAPK_gen_1 | 69 | 78 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 21 | 30 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 216 | 225 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 69 | 78 | PF00069 | 0.542 |
DOC_PP2B_LxvP_1 | 231 | 234 | PF13499 | 0.430 |
DOC_PP2B_LxvP_1 | 556 | 559 | PF13499 | 0.778 |
DOC_PP2B_LxvP_1 | 71 | 74 | PF13499 | 0.520 |
DOC_SPAK_OSR1_1 | 302 | 306 | PF12202 | 0.716 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.788 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.804 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.724 |
DOC_USP7_UBL2_3 | 252 | 256 | PF12436 | 0.657 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.524 |
LIG_14-3-3_CanoR_1 | 176 | 181 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 569 | 576 | PF00244 | 0.803 |
LIG_Clathr_ClatBox_1 | 117 | 121 | PF01394 | 0.457 |
LIG_EVH1_2 | 209 | 213 | PF00568 | 0.521 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.604 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.531 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.812 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.757 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.774 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.730 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.522 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.673 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.440 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.758 |
LIG_Integrin_RGD_1 | 537 | 539 | PF01839 | 0.584 |
LIG_LIR_Gen_1 | 282 | 291 | PF02991 | 0.744 |
LIG_LIR_Gen_1 | 301 | 311 | PF02991 | 0.587 |
LIG_LIR_Gen_1 | 35 | 43 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 515 | 525 | PF02991 | 0.710 |
LIG_LIR_Nem_3 | 282 | 286 | PF02991 | 0.735 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.718 |
LIG_LIR_Nem_3 | 515 | 520 | PF02991 | 0.706 |
LIG_NRBOX | 28 | 34 | PF00104 | 0.412 |
LIG_SH2_GRB2like | 456 | 459 | PF00017 | 0.734 |
LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.734 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.574 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.803 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.738 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.575 |
LIG_SH3_CIN85_PxpxPR_1 | 83 | 88 | PF14604 | 0.439 |
LIG_SUMO_SIM_anti_2 | 186 | 192 | PF11976 | 0.549 |
LIG_SUMO_SIM_anti_2 | 77 | 82 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 188 | 194 | PF11976 | 0.556 |
LIG_SUMO_SIM_par_1 | 29 | 35 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 74 | 79 | PF11976 | 0.455 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.524 |
LIG_TRAF2_1 | 380 | 383 | PF00917 | 0.781 |
LIG_WRC_WIRS_1 | 108 | 113 | PF05994 | 0.499 |
LIG_WRC_WIRS_1 | 33 | 38 | PF05994 | 0.375 |
LIG_WRC_WIRS_1 | 520 | 525 | PF05994 | 0.681 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.604 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.567 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.636 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.514 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.724 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.350 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.762 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.787 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.674 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.758 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.633 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.759 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.777 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.751 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.742 |
MOD_GlcNHglycan | 168 | 172 | PF01048 | 0.749 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.684 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.739 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.549 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.610 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.470 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.595 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.528 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.625 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.557 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.573 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.479 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.592 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.594 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.750 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.726 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.705 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.517 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.555 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.569 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.566 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.557 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.577 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.754 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.729 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.769 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.691 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.500 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.542 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.525 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.564 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.530 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.742 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.414 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.709 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.747 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.495 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.463 |
MOD_NEK2_2 | 171 | 176 | PF00069 | 0.512 |
MOD_NEK2_2 | 491 | 496 | PF00069 | 0.730 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.499 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.728 |
MOD_PKA_1 | 176 | 182 | PF00069 | 0.456 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.534 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.461 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.701 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.738 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.674 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.759 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.449 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.466 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.693 |
MOD_Plk_1 | 450 | 456 | PF00069 | 0.650 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.634 |
MOD_Plk_2-3 | 568 | 574 | PF00069 | 0.759 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.456 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.786 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.762 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.473 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.747 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.556 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.753 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.526 |
TRG_ER_diArg_1 | 175 | 177 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 247 | 250 | PF00400 | 0.712 |
TRG_ER_diArg_1 | 300 | 303 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 335 | 338 | PF00400 | 0.712 |
TRG_NLS_MonoExtC_3 | 251 | 256 | PF00514 | 0.651 |
TRG_NLS_MonoExtC_3 | 332 | 337 | PF00514 | 0.708 |
TRG_NLS_MonoExtN_4 | 250 | 257 | PF00514 | 0.651 |
TRG_NLS_MonoExtN_4 | 331 | 338 | PF00514 | 0.709 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ILH2 | Leishmania donovani | 88% | 97% |
A0A3S7WX43 | Leishmania donovani | 89% | 97% |
A4HCB1 | Leishmania braziliensis | 63% | 100% |
A4HDA2 | Leishmania braziliensis | 57% | 96% |
E9AGZ2 | Leishmania infantum | 89% | 97% |
E9AGZ3 | Leishmania infantum | 89% | 97% |
E9AVQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QBR2 | Leishmania major | 100% | 100% |