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: A4HTH2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 173 | 177 | PF00656 | 0.646 |
CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.624 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.770 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.646 |
CLV_PCSK_FUR_1 | 295 | 299 | PF00082 | 0.579 |
CLV_PCSK_FUR_1 | 410 | 414 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.779 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.750 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 117 | 119 | PF00082 | 0.686 |
CLV_PCSK_PC1ET2_1 | 460 | 462 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.691 |
DEG_SPOP_SBC_1 | 286 | 290 | PF00917 | 0.666 |
DOC_ANK_TNKS_1 | 104 | 111 | PF00023 | 0.647 |
DOC_MAPK_gen_1 | 410 | 420 | PF00069 | 0.590 |
DOC_MAPK_MEF2A_6 | 243 | 250 | PF00069 | 0.680 |
DOC_PP2B_LxvP_1 | 269 | 272 | PF13499 | 0.673 |
DOC_PP2B_LxvP_1 | 355 | 358 | PF13499 | 0.725 |
DOC_PP4_FxxP_1 | 251 | 254 | PF00568 | 0.618 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.604 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.562 |
LIG_14-3-3_CanoR_1 | 170 | 176 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 287 | 292 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 394 | 402 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 434 | 443 | PF00244 | 0.521 |
LIG_ActinCP_TwfCPI_2 | 251 | 258 | PF01115 | 0.625 |
LIG_APCC_ABBA_1 | 120 | 125 | PF00400 | 0.704 |
LIG_BIR_III_2 | 217 | 221 | PF00653 | 0.610 |
LIG_BIR_III_2 | 262 | 266 | PF00653 | 0.647 |
LIG_BRCT_BRCA1_1 | 438 | 442 | PF00533 | 0.706 |
LIG_deltaCOP1_diTrp_1 | 158 | 162 | PF00928 | 0.587 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.719 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.689 |
LIG_FHA_2 | 465 | 471 | PF00498 | 0.660 |
LIG_Integrin_RGD_1 | 107 | 109 | PF01839 | 0.669 |
LIG_Integrin_RGD_1 | 192 | 194 | PF01839 | 0.621 |
LIG_LIR_Apic_2 | 31 | 36 | PF02991 | 0.675 |
LIG_LIR_Apic_2 | 403 | 409 | PF02991 | 0.601 |
LIG_LIR_Gen_1 | 439 | 450 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.635 |
LIG_MYND_1 | 268 | 272 | PF01753 | 0.670 |
LIG_Pex14_2 | 442 | 446 | PF04695 | 0.628 |
LIG_PTAP_UEV_1 | 93 | 98 | PF05743 | 0.686 |
LIG_SH2_CRK | 33 | 37 | PF00017 | 0.623 |
LIG_SH2_SRC | 406 | 409 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.763 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.617 |
LIG_SH3_1 | 33 | 39 | PF00018 | 0.617 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.694 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.658 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.616 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.617 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.611 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.527 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.568 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.805 |
LIG_SUMO_SIM_par_1 | 266 | 274 | PF11976 | 0.711 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.701 |
LIG_TRAF2_1 | 56 | 59 | PF00917 | 0.725 |
LIG_TRAF2_1 | 83 | 86 | PF00917 | 0.665 |
LIG_TRFH_1 | 405 | 409 | PF08558 | 0.620 |
LIG_WW_3 | 1 | 5 | PF00397 | 0.657 |
LIG_WW_3 | 143 | 147 | PF00397 | 0.675 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.659 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.701 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.629 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.694 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.670 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.489 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.779 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.496 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.704 |
MOD_Cter_Amidation | 176 | 179 | PF01082 | 0.703 |
MOD_DYRK1A_RPxSP_1 | 264 | 268 | PF00069 | 0.642 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.680 |
MOD_GlcNHglycan | 124 | 130 | PF01048 | 0.635 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.713 |
MOD_GlcNHglycan | 282 | 286 | PF01048 | 0.728 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.742 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.626 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.691 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.671 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.534 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.736 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.707 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.666 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.797 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.656 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.743 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.806 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.626 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.782 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.671 |
MOD_LATS_1 | 182 | 188 | PF00433 | 0.593 |
MOD_N-GLC_1 | 278 | 283 | PF02516 | 0.681 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.702 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.764 |
MOD_NEK2_2 | 112 | 117 | PF00069 | 0.659 |
MOD_NEK2_2 | 28 | 33 | PF00069 | 0.718 |
MOD_PKA_1 | 298 | 304 | PF00069 | 0.721 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.644 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.651 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.736 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.641 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.561 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.738 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.637 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.554 |
MOD_Plk_1 | 304 | 310 | PF00069 | 0.607 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.607 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.643 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.514 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.660 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.745 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.630 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.567 |
TRG_DiLeu_BaLyEn_6 | 265 | 270 | PF01217 | 0.664 |
TRG_DiLeu_BaLyEn_6 | 373 | 378 | PF01217 | 0.635 |
TRG_ER_diArg_1 | 295 | 298 | PF00400 | 0.756 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.579 |
TRG_NLS_MonoExtC_3 | 211 | 217 | PF00514 | 0.674 |
TRG_NLS_MonoExtN_4 | 210 | 216 | PF00514 | 0.681 |
TRG_Pf-PMV_PEXEL_1 | 258 | 262 | PF00026 | 0.659 |
TRG_Pf-PMV_PEXEL_1 | 359 | 364 | PF00026 | 0.661 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H635 | Leishmania donovani | 99% | 100% |
A4H588 | Leishmania braziliensis | 51% | 100% |
E9AMA0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4QIE8 | Leishmania major | 87% | 100% |