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: 1 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9ADX8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.474 |
CLV_C14_Caspase3-7 | 239 | 243 | PF00656 | 0.490 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.628 |
CLV_PCSK_FUR_1 | 289 | 293 | PF00082 | 0.612 |
CLV_PCSK_FUR_1 | 51 | 55 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 127 | 129 | PF00082 | 0.686 |
CLV_PCSK_PC1ET2_1 | 197 | 199 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.441 |
DEG_APCC_DBOX_1 | 17 | 25 | PF00400 | 0.475 |
DEG_APCC_DBOX_1 | 195 | 203 | PF00400 | 0.469 |
DEG_APCC_DBOX_1 | 509 | 517 | PF00400 | 0.366 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.490 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 198 | 206 | PF00134 | 0.542 |
DOC_CYCLIN_yCln2_LP_2 | 183 | 189 | PF00134 | 0.501 |
DOC_CYCLIN_yCln2_LP_2 | 559 | 565 | PF00134 | 0.385 |
DOC_MAPK_gen_1 | 196 | 205 | PF00069 | 0.550 |
DOC_MAPK_gen_1 | 314 | 322 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 508 | 517 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 18 | 26 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 508 | 517 | PF00069 | 0.385 |
DOC_MAPK_NFAT4_5 | 508 | 516 | PF00069 | 0.385 |
DOC_PP2B_LxvP_1 | 183 | 186 | PF13499 | 0.501 |
DOC_PP2B_LxvP_1 | 559 | 562 | PF13499 | 0.385 |
DOC_PP4_FxxP_1 | 545 | 548 | PF00568 | 0.332 |
DOC_SPAK_OSR1_1 | 492 | 496 | PF12202 | 0.600 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.742 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.803 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.619 |
LIG_14-3-3_CanoR_1 | 12 | 19 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 149 | 154 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 248 | 255 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 492 | 502 | PF00244 | 0.707 |
LIG_Actin_WH2_2 | 558 | 575 | PF00022 | 0.385 |
LIG_BIR_III_4 | 386 | 390 | PF00653 | 0.685 |
LIG_deltaCOP1_diTrp_1 | 344 | 347 | PF00928 | 0.254 |
LIG_deltaCOP1_diTrp_1 | 367 | 376 | PF00928 | 0.778 |
LIG_EH1_1 | 354 | 362 | PF00400 | 0.342 |
LIG_EVH1_1 | 73 | 77 | PF00568 | 0.403 |
LIG_FAT_LD_1 | 199 | 207 | PF03623 | 0.445 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.446 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.533 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.527 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.457 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.766 |
LIG_GBD_Chelix_1 | 517 | 525 | PF00786 | 0.363 |
LIG_LIR_Gen_1 | 326 | 335 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 346 | 356 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 549 | 558 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.405 |
LIG_LIR_LC3C_4 | 556 | 561 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 344 | 348 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 524 | 529 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 549 | 553 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 556 | 561 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.511 |
LIG_MYND_1 | 439 | 443 | PF01753 | 0.637 |
LIG_NBox_RRM_1 | 347 | 357 | PF00076 | 0.342 |
LIG_NRBOX | 103 | 109 | PF00104 | 0.352 |
LIG_NRBOX | 198 | 204 | PF00104 | 0.565 |
LIG_NRBOX | 508 | 514 | PF00104 | 0.385 |
LIG_Pex14_1 | 273 | 277 | PF04695 | 0.464 |
LIG_Pex14_1 | 343 | 347 | PF04695 | 0.441 |
LIG_Pex14_2 | 546 | 550 | PF04695 | 0.363 |
LIG_REV1ctd_RIR_1 | 8 | 16 | PF16727 | 0.532 |
LIG_RPA_C_Fungi | 486 | 498 | PF08784 | 0.510 |
LIG_SH2_CRK | 227 | 231 | PF00017 | 0.753 |
LIG_SH2_CRK | 348 | 352 | PF00017 | 0.396 |
LIG_SH2_CRK | 461 | 465 | PF00017 | 0.627 |
LIG_SH2_NCK_1 | 348 | 352 | PF00017 | 0.254 |
LIG_SH2_STAP1 | 533 | 537 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.478 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.631 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.570 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.531 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.522 |
LIG_SUMO_SIM_anti_2 | 102 | 109 | PF11976 | 0.373 |
LIG_SUMO_SIM_par_1 | 102 | 109 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 204 | 212 | PF11976 | 0.460 |
LIG_TRAF2_1 | 578 | 581 | PF00917 | 0.499 |
LIG_TYR_ITSM | 344 | 351 | PF00017 | 0.320 |
LIG_UBA3_1 | 504 | 508 | PF00899 | 0.385 |
LIG_UBA3_1 | 565 | 573 | PF00899 | 0.469 |
LIG_WRC_WIRS_1 | 582 | 587 | PF05994 | 0.507 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.674 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.553 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.608 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.628 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.702 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.637 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.630 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.694 |
MOD_CMANNOS | 523 | 526 | PF00535 | 0.385 |
MOD_Cter_Amidation | 451 | 454 | PF01082 | 0.599 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.563 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.636 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.588 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.359 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.637 |
MOD_GlcNHglycan | 397 | 401 | PF01048 | 0.652 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.651 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.597 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.579 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.616 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.527 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.556 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.259 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.612 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.637 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.742 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.278 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.599 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.697 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.734 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.726 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.600 |
MOD_N-GLC_1 | 378 | 383 | PF02516 | 0.611 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.559 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.716 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.599 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.575 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.617 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.569 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.379 |
MOD_NEK2_2 | 343 | 348 | PF00069 | 0.320 |
MOD_PK_1 | 149 | 155 | PF00069 | 0.586 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.525 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.554 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.660 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.618 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.254 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.614 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.604 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.529 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.616 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.597 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.532 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.517 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.474 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.453 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.547 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.700 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.765 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.488 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.557 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.502 |
TRG_DiLeu_BaEn_1 | 103 | 108 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_1 | 233 | 238 | PF01217 | 0.632 |
TRG_DiLeu_BaEn_1 | 592 | 597 | PF01217 | 0.533 |
TRG_DiLeu_BaLyEn_6 | 507 | 512 | PF01217 | 0.385 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.630 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 196 | 199 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 213 | 215 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 489 | 492 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 53 | 55 | PF00400 | 0.519 |
TRG_NLS_MonoExtC_3 | 126 | 132 | PF00514 | 0.468 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IBG2 | Leishmania donovani | 92% | 100% |
A4HHD2 | Leishmania braziliensis | 68% | 100% |
A4I4H7 | Leishmania infantum | 92% | 100% |
E9ALV3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |