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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HKG3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.340 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.597 |
CLV_PCSK_FUR_1 | 2 | 6 | PF00082 | 0.547 |
CLV_PCSK_FUR_1 | 302 | 306 | PF00082 | 0.469 |
CLV_PCSK_FUR_1 | 358 | 362 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 505 | 507 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 360 | 362 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 505 | 507 | PF00082 | 0.561 |
CLV_PCSK_PC7_1 | 125 | 131 | PF00082 | 0.465 |
CLV_PCSK_PC7_1 | 356 | 362 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.724 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.466 |
DEG_APCC_DBOX_1 | 239 | 247 | PF00400 | 0.704 |
DEG_COP1_1 | 439 | 447 | PF00400 | 0.529 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.560 |
DEG_SPOP_SBC_1 | 264 | 268 | PF00917 | 0.486 |
DOC_ANK_TNKS_1 | 341 | 348 | PF00023 | 0.471 |
DOC_ANK_TNKS_1 | 360 | 367 | PF00023 | 0.532 |
DOC_MAPK_gen_1 | 2 | 9 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 382 | 391 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 148 | 157 | PF00069 | 0.418 |
DOC_PP2B_LxvP_1 | 389 | 392 | PF13499 | 0.458 |
DOC_PP2B_LxvP_1 | 42 | 45 | PF13499 | 0.464 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.468 |
DOC_USP7_UBL2_3 | 316 | 320 | PF12436 | 0.371 |
DOC_USP7_UBL2_3 | 376 | 380 | PF12436 | 0.642 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.525 |
LIG_14-3-3_CanoR_1 | 211 | 220 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 247 | 255 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 372 | 379 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 387 | 392 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 436 | 445 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 68 | 76 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 8 | 17 | PF00244 | 0.483 |
LIG_AP2alpha_1 | 63 | 67 | PF02296 | 0.366 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.339 |
LIG_BRCT_BRCA1_1 | 251 | 255 | PF00533 | 0.566 |
LIG_BRCT_BRCA1_1 | 33 | 37 | PF00533 | 0.616 |
LIG_Clathr_ClatBox_1 | 152 | 156 | PF01394 | 0.480 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.401 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.384 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.329 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.600 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.419 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.344 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.709 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.739 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.566 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.490 |
LIG_LIR_Gen_1 | 156 | 165 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 334 | 345 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 472 | 482 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 60 | 69 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 91 | 102 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 156 | 160 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 472 | 477 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.474 |
LIG_LYPXL_SIV_4 | 473 | 481 | PF13949 | 0.495 |
LIG_Pex14_1 | 185 | 189 | PF04695 | 0.339 |
LIG_Pex14_2 | 63 | 67 | PF04695 | 0.523 |
LIG_Rb_LxCxE_1 | 169 | 188 | PF01857 | 0.339 |
LIG_REV1ctd_RIR_1 | 64 | 72 | PF16727 | 0.487 |
LIG_RPA_C_Fungi | 118 | 130 | PF08784 | 0.341 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.371 |
LIG_SH2_PTP2 | 474 | 477 | PF00017 | 0.512 |
LIG_SH2_STAT3 | 242 | 245 | PF00017 | 0.592 |
LIG_SH2_STAT3 | 349 | 352 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.403 |
LIG_SH3_2 | 45 | 50 | PF14604 | 0.542 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.576 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.564 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.524 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.568 |
LIG_Sin3_3 | 115 | 122 | PF02671 | 0.499 |
LIG_SUMO_SIM_par_1 | 15 | 20 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 151 | 156 | PF11976 | 0.434 |
LIG_TRAF2_1 | 350 | 353 | PF00917 | 0.626 |
LIG_TRAF2_1 | 412 | 415 | PF00917 | 0.663 |
LIG_TRAF2_1 | 77 | 80 | PF00917 | 0.530 |
LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.396 |
LIG_UBA3_1 | 132 | 138 | PF00899 | 0.495 |
MOD_CDC14_SPxK_1 | 20 | 23 | PF00782 | 0.487 |
MOD_CDK_SPxK_1 | 17 | 23 | PF00069 | 0.485 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.548 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.686 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.475 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.604 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.592 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.674 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.336 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.501 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.815 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.716 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.547 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.503 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.489 |
MOD_Cter_Amidation | 2 | 5 | PF01082 | 0.546 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.504 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.562 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.597 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.541 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.587 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.557 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.525 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.560 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.691 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.815 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.460 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.329 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.646 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.563 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.592 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.569 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.443 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.745 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.606 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.589 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.387 |
MOD_N-GLC_1 | 456 | 461 | PF02516 | 0.689 |
MOD_N-GLC_2 | 495 | 497 | PF02516 | 0.423 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.545 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.688 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.349 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.442 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.565 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.602 |
MOD_NEK2_2 | 78 | 83 | PF00069 | 0.333 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.647 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.349 |
MOD_PK_1 | 232 | 238 | PF00069 | 0.466 |
MOD_PK_1 | 387 | 393 | PF00069 | 0.439 |
MOD_PKA_1 | 205 | 211 | PF00069 | 0.634 |
MOD_PKA_1 | 212 | 218 | PF00069 | 0.649 |
MOD_PKA_1 | 436 | 442 | PF00069 | 0.587 |
MOD_PKA_1 | 505 | 511 | PF00069 | 0.473 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.641 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.638 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.674 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.528 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.652 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.647 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.659 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.673 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.473 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.349 |
MOD_PKB_1 | 385 | 393 | PF00069 | 0.431 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.548 |
MOD_Plk_1 | 332 | 338 | PF00069 | 0.331 |
MOD_Plk_1 | 498 | 504 | PF00069 | 0.527 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.358 |
MOD_Plk_2-3 | 400 | 406 | PF00069 | 0.523 |
MOD_Plk_2-3 | 54 | 60 | PF00069 | 0.447 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.596 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.532 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.467 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.574 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.580 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.504 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.584 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.528 |
TRG_DiLeu_BaEn_1 | 113 | 118 | PF01217 | 0.555 |
TRG_DiLeu_BaEn_1 | 156 | 161 | PF01217 | 0.484 |
TRG_DiLeu_BaEn_4 | 174 | 180 | PF01217 | 0.376 |
TRG_DiLeu_BaEn_4 | 414 | 420 | PF01217 | 0.535 |
TRG_DiLeu_BaLyEn_6 | 273 | 278 | PF01217 | 0.614 |
TRG_DiLeu_BaLyEn_6 | 339 | 344 | PF01217 | 0.331 |
TRG_DiLeu_BaLyEn_6 | 379 | 384 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 482 | 487 | PF01217 | 0.489 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.549 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 129 | 131 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 205 | 207 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 295 | 298 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 302 | 305 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 384 | 387 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 435 | 437 | PF00400 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 342 | 346 | PF00026 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 382 | 386 | PF00026 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMW1 | Leptomonas seymouri | 42% | 89% |
A0A3Q8IG72 | Leishmania donovani | 62% | 100% |
A0A3R7MFC1 | Trypanosoma rangeli | 25% | 87% |
A4I7Z1 | Leishmania infantum | 62% | 100% |
E9B2V2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 100% |
Q4Q5A4 | Leishmania major | 59% | 98% |