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 | yes | 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: A0A3S7WX43
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 383 | 387 | PF00656 | 0.688 |
CLV_C14_Caspase3-7 | 538 | 542 | PF00656 | 0.823 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.496 |
CLV_PCSK_FUR_1 | 249 | 253 | PF00082 | 0.448 |
CLV_PCSK_FUR_1 | 334 | 338 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 251 | 253 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.517 |
CLV_PCSK_PC7_1 | 247 | 253 | PF00082 | 0.442 |
CLV_PCSK_PC7_1 | 332 | 338 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.488 |
DEG_APCC_DBOX_1 | 220 | 228 | PF00400 | 0.388 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.661 |
DEG_SCF_FBW7_1 | 151 | 157 | PF00400 | 0.475 |
DEG_SPOP_SBC_1 | 128 | 132 | PF00917 | 0.528 |
DEG_SPOP_SBC_1 | 154 | 158 | PF00917 | 0.518 |
DEG_SPOP_SBC_1 | 201 | 205 | PF00917 | 0.540 |
DEG_SPOP_SBC_1 | 437 | 441 | PF00917 | 0.727 |
DOC_CKS1_1 | 151 | 156 | PF01111 | 0.475 |
DOC_CKS1_1 | 43 | 48 | PF01111 | 0.606 |
DOC_CYCLIN_RxL_1 | 173 | 182 | PF00134 | 0.427 |
DOC_CYCLIN_RxL_1 | 249 | 262 | PF00134 | 0.721 |
DOC_CYCLIN_RxL_1 | 458 | 468 | PF00134 | 0.644 |
DOC_CYCLIN_yCln2_LP_2 | 230 | 236 | PF00134 | 0.441 |
DOC_CYCLIN_yCln2_LP_2 | 80 | 86 | PF00134 | 0.556 |
DOC_MAPK_gen_1 | 215 | 222 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 249 | 259 | PF00069 | 0.710 |
DOC_MAPK_gen_1 | 330 | 340 | PF00069 | 0.720 |
DOC_MAPK_gen_1 | 69 | 78 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 215 | 224 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 25 | 32 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 69 | 78 | PF00069 | 0.554 |
DOC_PP2B_LxvP_1 | 178 | 181 | PF13499 | 0.421 |
DOC_PP2B_LxvP_1 | 230 | 233 | PF13499 | 0.441 |
DOC_PP2B_LxvP_1 | 555 | 558 | PF13499 | 0.785 |
DOC_PP2B_LxvP_1 | 71 | 74 | PF13499 | 0.530 |
DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.501 |
DOC_SPAK_OSR1_1 | 301 | 305 | PF12202 | 0.722 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.792 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.656 |
DOC_USP7_UBL2_3 | 251 | 255 | PF12436 | 0.669 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.641 |
LIG_14-3-3_CanoR_1 | 16 | 23 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 166 | 174 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 175 | 179 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 568 | 575 | PF00244 | 0.764 |
LIG_EVH1_2 | 208 | 212 | PF00568 | 0.532 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.576 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.811 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.729 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.629 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.422 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.533 |
LIG_FHA_2 | 568 | 574 | PF00498 | 0.765 |
LIG_Integrin_isoDGR_2 | 141 | 143 | PF01839 | 0.718 |
LIG_Integrin_RGD_1 | 47 | 49 | PF01839 | 0.652 |
LIG_Integrin_RGD_1 | 536 | 538 | PF01839 | 0.587 |
LIG_LIR_Apic_2 | 598 | 602 | PF02991 | 0.634 |
LIG_LIR_Gen_1 | 281 | 290 | PF02991 | 0.759 |
LIG_LIR_Gen_1 | 35 | 43 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 514 | 524 | PF02991 | 0.773 |
LIG_LIR_Nem_3 | 281 | 285 | PF02991 | 0.754 |
LIG_LIR_Nem_3 | 316 | 322 | PF02991 | 0.664 |
LIG_LIR_Nem_3 | 514 | 519 | PF02991 | 0.768 |
LIG_MYND_1 | 79 | 83 | PF01753 | 0.472 |
LIG_NRBOX | 28 | 34 | PF00104 | 0.541 |
LIG_SH2_GRB2like | 455 | 458 | PF00017 | 0.748 |
LIG_SH2_SRC | 611 | 614 | PF00017 | 0.714 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.748 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.669 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.714 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.482 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.604 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.794 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.740 |
LIG_SH3_3 | 607 | 613 | PF00018 | 0.679 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.549 |
LIG_SUMO_SIM_anti_2 | 185 | 191 | PF11976 | 0.554 |
LIG_SUMO_SIM_par_1 | 187 | 193 | PF11976 | 0.556 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.532 |
LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.797 |
LIG_WRC_WIRS_1 | 108 | 113 | PF05994 | 0.507 |
LIG_WRC_WIRS_1 | 33 | 38 | PF05994 | 0.531 |
LIG_WRC_WIRS_1 | 519 | 524 | PF05994 | 0.689 |
MOD_CDK_SPK_2 | 11 | 16 | PF00069 | 0.610 |
MOD_CDK_SPK_2 | 42 | 47 | PF00069 | 0.533 |
MOD_CDK_SPxK_1 | 286 | 292 | PF00069 | 0.678 |
MOD_CDK_SPxxK_3 | 214 | 221 | PF00069 | 0.405 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.590 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.547 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.588 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.503 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.733 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.552 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.838 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.825 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.766 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.636 |
MOD_CK2_1 | 567 | 573 | PF00069 | 0.766 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.818 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.716 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.743 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.656 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.788 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.567 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.571 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.511 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.611 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.632 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.565 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.509 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.558 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.555 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.740 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.554 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.729 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.681 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.536 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.527 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.474 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.477 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.685 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.595 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.738 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.786 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.689 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.432 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.679 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.723 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.552 |
MOD_N-GLC_1 | 456 | 461 | PF02516 | 0.576 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.517 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.563 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.752 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.575 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.721 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.536 |
MOD_NEK2_2 | 170 | 175 | PF00069 | 0.512 |
MOD_NEK2_2 | 490 | 495 | PF00069 | 0.738 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.506 |
MOD_PIKK_1 | 600 | 606 | PF00454 | 0.678 |
MOD_PK_1 | 511 | 517 | PF00069 | 0.634 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.561 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.631 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.540 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.466 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.661 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.721 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.667 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.688 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.766 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.720 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.689 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.672 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.673 |
MOD_Plk_2-3 | 567 | 573 | PF00069 | 0.766 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.796 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.726 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.646 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.667 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.584 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.485 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.426 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.681 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.762 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.643 |
TRG_DiLeu_BaLyEn_6 | 76 | 81 | PF01217 | 0.471 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.722 |
TRG_ER_diArg_1 | 560 | 563 | PF00400 | 0.695 |
TRG_NLS_MonoExtC_3 | 250 | 255 | PF00514 | 0.662 |
TRG_NLS_MonoExtC_3 | 331 | 336 | PF00514 | 0.720 |
TRG_NLS_MonoExtN_4 | 249 | 256 | PF00514 | 0.662 |
TRG_NLS_MonoExtN_4 | 330 | 337 | PF00514 | 0.720 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ILH2 | Leishmania donovani | 99% | 100% |
A4HCB1 | Leishmania braziliensis | 63% | 100% |
A4HDA2 | Leishmania braziliensis | 57% | 100% |
E9AGZ2 | Leishmania infantum | 98% | 100% |
E9AGZ3 | Leishmania infantum | 98% | 100% |
E9AVQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QBR2 | Leishmania major | 89% | 100% |
Q4QBS8 | Leishmania major | 89% | 100% |