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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: E9AKG2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 146 | 150 | PF00656 | 0.665 |
CLV_C14_Caspase3-7 | 15 | 19 | PF00656 | 0.442 |
CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.670 |
CLV_C14_Caspase3-7 | 343 | 347 | PF00656 | 0.701 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.666 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.666 |
CLV_PCSK_PC1ET2_1 | 358 | 360 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.735 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.585 |
DEG_SPOP_SBC_1 | 103 | 107 | PF00917 | 0.753 |
DOC_MAPK_gen_1 | 358 | 364 | PF00069 | 0.598 |
DOC_MAPK_MEF2A_6 | 358 | 366 | PF00069 | 0.612 |
DOC_MAPK_NFAT4_5 | 363 | 371 | PF00069 | 0.480 |
DOC_MAPK_RevD_3 | 367 | 383 | PF00069 | 0.285 |
DOC_PP2B_LxvP_1 | 215 | 218 | PF13499 | 0.654 |
DOC_PP4_MxPP_1 | 321 | 324 | PF00568 | 0.595 |
DOC_SPAK_OSR1_1 | 125 | 129 | PF12202 | 0.565 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.658 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.785 |
LIG_14-3-3_CanoR_1 | 100 | 104 | PF00244 | 0.751 |
LIG_14-3-3_CanoR_1 | 111 | 120 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 152 | 160 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 223 | 233 | PF00244 | 0.738 |
LIG_14-3-3_CanoR_1 | 234 | 239 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 290 | 298 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 382 | 391 | PF00244 | 0.493 |
LIG_APCC_ABBA_1 | 182 | 187 | PF00400 | 0.570 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.527 |
LIG_BRCT_BRCA1_1 | 36 | 40 | PF00533 | 0.547 |
LIG_EH1_1 | 364 | 372 | PF00400 | 0.426 |
LIG_eIF4E_1 | 365 | 371 | PF01652 | 0.426 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.620 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.677 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.805 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.602 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.213 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.581 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.497 |
LIG_LIR_Gen_1 | 129 | 138 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 332 | 342 | PF02991 | 0.745 |
LIG_LIR_Gen_1 | 373 | 381 | PF02991 | 0.401 |
LIG_LIR_LC3C_4 | 212 | 217 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 129 | 133 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.744 |
LIG_LIR_Nem_3 | 373 | 378 | PF02991 | 0.355 |
LIG_MYND_1 | 239 | 243 | PF01753 | 0.739 |
LIG_SH2_CRK | 365 | 369 | PF00017 | 0.383 |
LIG_SH2_CRK | 56 | 60 | PF00017 | 0.538 |
LIG_SH2_PTP2 | 130 | 133 | PF00017 | 0.584 |
LIG_SH2_PTP2 | 375 | 378 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.707 |
LIG_SH2_STAP1 | 406 | 410 | PF00017 | 0.537 |
LIG_SH2_STAT3 | 406 | 409 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.347 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.752 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.544 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.644 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.586 |
LIG_SH3_4 | 311 | 318 | PF00018 | 0.614 |
LIG_Sin3_3 | 213 | 220 | PF02671 | 0.636 |
LIG_SUMO_SIM_par_1 | 368 | 373 | PF11976 | 0.293 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.658 |
LIG_TRAF2_1 | 401 | 404 | PF00917 | 0.447 |
LIG_TYR_ITIM | 128 | 133 | PF00017 | 0.562 |
MOD_CDK_SPK_2 | 241 | 246 | PF00069 | 0.800 |
MOD_CDK_SPK_2 | 285 | 290 | PF00069 | 0.666 |
MOD_CDK_SPK_2 | 408 | 413 | PF00069 | 0.382 |
MOD_CDK_SPxxK_3 | 304 | 311 | PF00069 | 0.763 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.679 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.726 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.793 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.677 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.766 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.712 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.489 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.536 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.537 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.414 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.506 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.494 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.567 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.556 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.425 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.788 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.554 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.728 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.590 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.648 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.706 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.720 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.486 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.630 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.486 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.773 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.602 |
MOD_N-GLC_1 | 34 | 39 | PF02516 | 0.407 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.412 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.620 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.789 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.606 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.563 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.324 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.671 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.652 |
MOD_PIKK_1 | 412 | 418 | PF00454 | 0.381 |
MOD_PKA_1 | 283 | 289 | PF00069 | 0.730 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.725 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.564 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.742 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.381 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.675 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.757 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.601 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.680 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.605 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.664 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.556 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.288 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.743 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.777 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.739 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.768 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.383 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.669 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.788 |
MOD_SUMO_for_1 | 133 | 136 | PF00179 | 0.598 |
MOD_SUMO_rev_2 | 389 | 393 | PF00179 | 0.378 |
TRG_DiLeu_BaEn_4 | 403 | 409 | PF01217 | 0.385 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.740 |
TRG_ENDOCYTIC_2 | 365 | 368 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.538 |
TRG_ER_diArg_1 | 233 | 236 | PF00400 | 0.788 |
TRG_ER_diArg_1 | 282 | 284 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 381 | 383 | PF00400 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 14 | 18 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 273 | 277 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2J2 | Leptomonas seymouri | 52% | 100% |
A0A0S4IL26 | Bodo saltans | 25% | 100% |
A0A1X0NKC1 | Trypanosomatidae | 34% | 100% |
A0A3S5H5I5 | Leishmania donovani | 86% | 100% |
A0A422ND80 | Trypanosoma rangeli | 31% | 100% |
A4H4A2 | Leishmania braziliensis | 71% | 99% |
A4HSH8 | Leishmania infantum | 86% | 100% |
Q4QJE6 | Leishmania major | 84% | 100% |
V5BAR1 | Trypanosoma cruzi | 29% | 100% |