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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4HC43
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.686 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.758 |
CLV_PCSK_PC7_1 | 492 | 498 | PF00082 | 0.752 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.583 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.589 |
DOC_CKS1_1 | 363 | 368 | PF01111 | 0.470 |
DOC_CYCLIN_yCln2_LP_2 | 70 | 73 | PF00134 | 0.511 |
DOC_PP2B_LxvP_1 | 70 | 73 | PF13499 | 0.511 |
DOC_PP4_FxxP_1 | 42 | 45 | PF00568 | 0.626 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.763 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 205 | 215 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 344 | 348 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 403 | 409 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 74 | 79 | PF00244 | 0.775 |
LIG_BIR_III_2 | 418 | 422 | PF00653 | 0.767 |
LIG_Clathr_ClatBox_1 | 368 | 372 | PF01394 | 0.743 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.752 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.638 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.588 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.666 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.729 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.581 |
LIG_GBD_Chelix_1 | 400 | 408 | PF00786 | 0.548 |
LIG_LIR_Gen_1 | 193 | 202 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.458 |
LIG_NRBOX | 131 | 137 | PF00104 | 0.765 |
LIG_NRBOX | 302 | 308 | PF00104 | 0.563 |
LIG_SH2_NCK_1 | 196 | 200 | PF00017 | 0.461 |
LIG_SH2_SRC | 196 | 199 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.522 |
LIG_SH3_1 | 360 | 366 | PF00018 | 0.442 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.694 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.641 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.716 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.532 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.637 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.767 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.532 |
LIG_SUMO_SIM_par_1 | 304 | 310 | PF11976 | 0.596 |
LIG_SUMO_SIM_par_1 | 367 | 373 | PF11976 | 0.724 |
LIG_TRAF2_1 | 275 | 278 | PF00917 | 0.710 |
LIG_WW_3 | 71 | 75 | PF00397 | 0.511 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.765 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.651 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.538 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.440 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.543 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.615 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.606 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.708 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.392 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.565 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.725 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.650 |
MOD_DYRK1A_RPxSP_1 | 208 | 212 | PF00069 | 0.471 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.765 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.710 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.538 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.620 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.677 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.713 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.611 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.729 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.756 |
MOD_GlcNHglycan | 467 | 471 | PF01048 | 0.723 |
MOD_GlcNHglycan | 478 | 482 | PF01048 | 0.582 |
MOD_GlcNHglycan | 85 | 89 | PF01048 | 0.791 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.743 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.792 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.524 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.578 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.494 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.730 |
MOD_N-GLC_1 | 376 | 381 | PF02516 | 0.678 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.614 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.660 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.504 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.583 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.745 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.739 |
MOD_NEK2_2 | 343 | 348 | PF00069 | 0.600 |
MOD_PIKK_1 | 16 | 22 | PF00454 | 0.678 |
MOD_PKA_1 | 496 | 502 | PF00069 | 0.739 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.736 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.724 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.579 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.609 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.706 |
MOD_PKB_1 | 331 | 339 | PF00069 | 0.421 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.580 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.368 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.351 |
MOD_Plk_2-3 | 392 | 398 | PF00069 | 0.438 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.765 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.751 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.605 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.734 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.753 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.688 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.725 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.462 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.635 |
TRG_DiLeu_BaEn_1 | 156 | 161 | PF01217 | 0.582 |
TRG_DiLeu_LyEn_5 | 156 | 161 | PF01217 | 0.628 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.461 |
TRG_ER_diArg_1 | 11 | 14 | PF00400 | 0.680 |
TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 494 | 497 | PF00400 | 0.756 |
TRG_ER_diArg_1 | 500 | 503 | PF00400 | 0.717 |
TRG_Pf-PMV_PEXEL_1 | 178 | 182 | PF00026 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 345 | 349 | PF00026 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK83 | Leptomonas seymouri | 43% | 100% |
A0A3S5H6A2 | Leishmania donovani | 74% | 100% |
A0A422NFT6 | Trypanosoma rangeli | 30% | 100% |
E9AG89 | Leishmania infantum | 70% | 100% |
E9AMJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4QI40 | Leishmania major | 73% | 99% |
V5AUD8 | Trypanosoma cruzi | 30% | 100% |