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: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HX13
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.630 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.748 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.662 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 438 | 440 | PF00082 | 0.742 |
CLV_PCSK_PC7_1 | 154 | 160 | PF00082 | 0.743 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.702 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.717 |
CLV_Separin_Metazoa | 21 | 25 | PF03568 | 0.612 |
DEG_APCC_DBOX_1 | 237 | 245 | PF00400 | 0.639 |
DEG_APCC_DBOX_1 | 299 | 307 | PF00400 | 0.666 |
DEG_APCC_DBOX_1 | 402 | 410 | PF00400 | 0.472 |
DOC_CKS1_1 | 215 | 220 | PF01111 | 0.565 |
DOC_CKS1_1 | 306 | 311 | PF01111 | 0.658 |
DOC_CYCLIN_RxL_1 | 235 | 245 | PF00134 | 0.700 |
DOC_CYCLIN_yCln2_LP_2 | 215 | 221 | PF00134 | 0.569 |
DOC_MAPK_gen_1 | 24 | 32 | PF00069 | 0.552 |
DOC_MAPK_MEF2A_6 | 399 | 406 | PF00069 | 0.590 |
DOC_MAPK_NFAT4_5 | 399 | 407 | PF00069 | 0.594 |
DOC_MAPK_RevD_3 | 469 | 484 | PF00069 | 0.458 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.718 |
DOC_PP4_FxxP_1 | 3 | 6 | PF00568 | 0.643 |
DOC_PP4_FxxP_1 | 95 | 98 | PF00568 | 0.733 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.613 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.769 |
LIG_14-3-3_CanoR_1 | 334 | 341 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 354 | 359 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 374 | 380 | PF00244 | 0.485 |
LIG_APCC_ABBA_1 | 23 | 28 | PF00400 | 0.634 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.628 |
LIG_eIF4E_1 | 113 | 119 | PF01652 | 0.510 |
LIG_EVH1_1 | 3 | 7 | PF00568 | 0.515 |
LIG_EVH1_2 | 180 | 184 | PF00568 | 0.720 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.675 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.723 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.705 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.618 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.598 |
LIG_LIR_Apic_2 | 2 | 6 | PF02991 | 0.649 |
LIG_LIR_Apic_2 | 92 | 98 | PF02991 | 0.733 |
LIG_LIR_Gen_1 | 247 | 257 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 342 | 353 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.505 |
LIG_NRBOX | 114 | 120 | PF00104 | 0.509 |
LIG_PCNA_yPIPBox_3 | 19 | 27 | PF02747 | 0.617 |
LIG_SH2_CRK | 422 | 426 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.652 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.677 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.724 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.610 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.728 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.704 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.626 |
LIG_SUMO_SIM_anti_2 | 250 | 255 | PF11976 | 0.464 |
LIG_TRFH_1 | 3 | 7 | PF08558 | 0.515 |
LIG_TYR_ITIM | 222 | 227 | PF00017 | 0.702 |
LIG_UBA3_1 | 252 | 261 | PF00899 | 0.599 |
MOD_CDK_SPK_2 | 364 | 369 | PF00069 | 0.645 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.635 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.667 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.649 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.520 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.592 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.752 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.611 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.499 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.759 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.784 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.615 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.658 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.634 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.507 |
MOD_GlcNHglycan | 140 | 144 | PF01048 | 0.676 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.728 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.759 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.619 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.662 |
MOD_GlcNHglycan | 83 | 87 | PF01048 | 0.612 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.562 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.656 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.642 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.554 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.740 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.689 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.548 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.710 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.443 |
MOD_N-GLC_2 | 172 | 174 | PF02516 | 0.624 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.440 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.662 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.608 |
MOD_PKA_1 | 374 | 380 | PF00069 | 0.691 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.581 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.763 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.747 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.691 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.593 |
MOD_PKB_1 | 439 | 447 | PF00069 | 0.690 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.438 |
MOD_Plk_2-3 | 136 | 142 | PF00069 | 0.774 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.706 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.415 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.622 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.634 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.690 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.696 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.557 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.690 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.582 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.642 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.767 |
TRG_DiLeu_BaEn_1 | 38 | 43 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 235 | 240 | PF01217 | 0.613 |
TRG_DiLeu_BaLyEn_6 | 377 | 382 | PF01217 | 0.637 |
TRG_DiLeu_LyEn_5 | 38 | 43 | PF01217 | 0.557 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.699 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.575 |
TRG_ER_diArg_1 | 168 | 170 | PF00400 | 0.705 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.662 |
TRG_NLS_MonoCore_2 | 437 | 442 | PF00514 | 0.746 |
TRG_NLS_MonoExtC_3 | 322 | 327 | PF00514 | 0.657 |
TRG_NLS_MonoExtC_3 | 437 | 443 | PF00514 | 0.748 |
TRG_NLS_MonoExtN_4 | 435 | 442 | PF00514 | 0.740 |
TRG_Pf-PMV_PEXEL_1 | 194 | 198 | PF00026 | 0.564 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Q0 | Leptomonas seymouri | 32% | 100% |
A0A3Q8IAM2 | Leishmania donovani | 100% | 100% |
A4H8P3 | Leishmania braziliensis | 72% | 99% |
E9AQS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QEQ1 | Leishmania major | 90% | 99% |