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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4H588
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 388 | 392 | PF00656 | 0.561 |
CLV_C14_Caspase3-7 | 45 | 49 | PF00656 | 0.555 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.573 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.779 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.572 |
CLV_PCSK_FUR_1 | 435 | 439 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.788 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 117 | 119 | PF00082 | 0.693 |
CLV_PCSK_PC1ET2_1 | 231 | 233 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.614 |
CLV_Separin_Metazoa | 394 | 398 | PF03568 | 0.589 |
DEG_APCC_DBOX_1 | 473 | 481 | PF00400 | 0.482 |
DOC_MAPK_gen_1 | 263 | 270 | PF00069 | 0.581 |
DOC_MAPK_gen_1 | 397 | 406 | PF00069 | 0.547 |
DOC_MAPK_gen_1 | 435 | 445 | PF00069 | 0.600 |
DOC_MAPK_MEF2A_6 | 263 | 270 | PF00069 | 0.714 |
DOC_PP2B_LxvP_1 | 375 | 378 | PF13499 | 0.706 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.554 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.564 |
DOC_USP7_UBL2_3 | 163 | 167 | PF12436 | 0.554 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.568 |
LIG_14-3-3_CanoR_1 | 299 | 307 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 399 | 405 | PF00244 | 0.564 |
LIG_14-3-3_CterR_2 | 524 | 527 | PF00244 | 0.566 |
LIG_Actin_WH2_2 | 463 | 480 | PF00022 | 0.455 |
LIG_APCC_ABBA_1 | 120 | 125 | PF00400 | 0.695 |
LIG_BRCT_BRCA1_1 | 463 | 467 | PF00533 | 0.649 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.540 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.704 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.549 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.705 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.540 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.524 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.585 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.448 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.631 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.611 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.593 |
LIG_Integrin_RGD_1 | 180 | 182 | PF01839 | 0.575 |
LIG_LIR_Apic_2 | 116 | 122 | PF02991 | 0.552 |
LIG_LIR_Apic_2 | 31 | 36 | PF02991 | 0.678 |
LIG_LIR_Apic_2 | 428 | 434 | PF02991 | 0.650 |
LIG_LIR_Gen_1 | 125 | 135 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 464 | 475 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 501 | 512 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 501 | 507 | PF02991 | 0.495 |
LIG_PDZ_Class_1 | 522 | 527 | PF00595 | 0.562 |
LIG_Pex14_2 | 467 | 471 | PF04695 | 0.586 |
LIG_PTAP_UEV_1 | 93 | 98 | PF05743 | 0.687 |
LIG_SH2_PTP2 | 128 | 131 | PF00017 | 0.513 |
LIG_SH2_SRC | 431 | 434 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.762 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.464 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.806 |
LIG_SUMO_SIM_anti_2 | 124 | 133 | PF11976 | 0.517 |
LIG_SUMO_SIM_anti_2 | 286 | 294 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 288 | 294 | PF11976 | 0.684 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.688 |
LIG_TRAF2_1 | 203 | 206 | PF00917 | 0.575 |
LIG_TRAF2_1 | 345 | 348 | PF00917 | 0.566 |
LIG_TRAF2_1 | 56 | 59 | PF00917 | 0.686 |
LIG_TRAF2_1 | 70 | 73 | PF00917 | 0.593 |
LIG_TRFH_1 | 430 | 434 | PF08558 | 0.664 |
LIG_ULM_U2AF65_1 | 230 | 235 | PF00076 | 0.558 |
MOD_CDK_SPK_2 | 184 | 189 | PF00069 | 0.580 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.573 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.548 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.628 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.691 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.624 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.604 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.541 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.554 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.634 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.570 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.393 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.520 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.564 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.675 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.661 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.796 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.656 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.605 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.640 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.551 |
MOD_GlcNHglycan | 302 | 306 | PF01048 | 0.723 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.677 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.659 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.686 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.571 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.579 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.603 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.712 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.762 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.526 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.642 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.600 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.652 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.669 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.541 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.678 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.506 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.574 |
MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.546 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.571 |
MOD_N-GLC_1 | 50 | 55 | PF02516 | 0.568 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.561 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.526 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.702 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.584 |
MOD_NEK2_2 | 28 | 33 | PF00069 | 0.703 |
MOD_PIKK_1 | 383 | 389 | PF00454 | 0.561 |
MOD_PK_1 | 502 | 508 | PF00069 | 0.432 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.621 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.586 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.764 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.505 |
MOD_PKB_1 | 397 | 405 | PF00069 | 0.548 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.570 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.619 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.552 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.566 |
MOD_Plk_2-3 | 276 | 282 | PF00069 | 0.567 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.628 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.619 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.580 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.674 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.737 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.615 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.580 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.563 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.580 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 232 | 234 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 434 | 437 | PF00400 | 0.602 |
TRG_NLS_MonoCore_2 | 229 | 234 | PF00514 | 0.560 |
TRG_NLS_MonoExtC_3 | 229 | 235 | PF00514 | 0.713 |
TRG_NLS_MonoExtN_4 | 227 | 234 | PF00514 | 0.712 |
TRG_Pf-PMV_PEXEL_1 | 446 | 450 | PF00026 | 0.534 |
TRG_PTS1 | 524 | 527 | PF00515 | 0.566 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H635 | Leishmania donovani | 51% | 100% |
A4HTH2 | Leishmania infantum | 51% | 100% |
E9AMA0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
Q4QIE8 | Leishmania major | 50% | 98% |