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: E9AG91
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 346 | 350 | PF00656 | 0.737 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.650 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.756 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.647 |
DEG_SPOP_SBC_1 | 19 | 23 | PF00917 | 0.739 |
DOC_MAPK_gen_1 | 270 | 276 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 87 | 95 | PF00069 | 0.663 |
DOC_MAPK_MEF2A_6 | 257 | 265 | PF00069 | 0.581 |
DOC_PP4_FxxP_1 | 295 | 298 | PF00568 | 0.547 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.728 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.728 |
LIG_14-3-3_CanoR_1 | 304 | 313 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 329 | 335 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 408 | 415 | PF00244 | 0.446 |
LIG_APCC_ABBA_1 | 387 | 392 | PF00400 | 0.554 |
LIG_BIR_III_2 | 349 | 353 | PF00653 | 0.647 |
LIG_CSL_BTD_1 | 421 | 424 | PF09270 | 0.566 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.711 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.572 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.644 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.624 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.607 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.618 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.590 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.692 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.540 |
LIG_GBD_Chelix_1 | 261 | 269 | PF00786 | 0.621 |
LIG_LIR_Apic_2 | 373 | 379 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 36 | 44 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 381 | 389 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.635 |
LIG_PCNA_yPIPBox_3 | 243 | 257 | PF02747 | 0.642 |
LIG_PDZ_Class_2 | 427 | 432 | PF00595 | 0.611 |
LIG_PDZ_Wminus1_1 | 430 | 432 | PF00595 | 0.618 |
LIG_Pex14_2 | 295 | 299 | PF04695 | 0.421 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.624 |
LIG_SH2_PTP2 | 148 | 151 | PF00017 | 0.594 |
LIG_SH2_PTP2 | 376 | 379 | PF00017 | 0.580 |
LIG_SH2_PTP2 | 39 | 42 | PF00017 | 0.618 |
LIG_SH2_SRC | 376 | 379 | PF00017 | 0.580 |
LIG_SH2_SRC | 39 | 42 | PF00017 | 0.618 |
LIG_SH2_STAP1 | 318 | 322 | PF00017 | 0.721 |
LIG_SH2_STAP1 | 52 | 56 | PF00017 | 0.672 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.626 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.644 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.605 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.752 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.589 |
LIG_SUMO_SIM_par_1 | 92 | 98 | PF11976 | 0.697 |
LIG_WRC_WIRS_1 | 331 | 336 | PF05994 | 0.551 |
LIG_WW_1 | 144 | 147 | PF00397 | 0.652 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.668 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.749 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.708 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.754 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.544 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.592 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.730 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.674 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.534 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.763 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.715 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.481 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.720 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.721 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.505 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.733 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.687 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.510 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.712 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.688 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.746 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.688 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.684 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.713 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.671 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.535 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.693 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.628 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.764 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.621 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.487 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.554 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.551 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.521 |
MOD_OFUCOSY | 111 | 116 | PF10250 | 0.647 |
MOD_PIKK_1 | 205 | 211 | PF00454 | 0.730 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.605 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.668 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.646 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.631 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.618 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.652 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.688 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.616 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.677 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.379 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.754 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.598 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.686 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.734 |
TRG_DiLeu_BaEn_1 | 326 | 331 | PF01217 | 0.642 |
TRG_DiLeu_LyEn_5 | 326 | 331 | PF01217 | 0.642 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.611 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.626 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.628 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.618 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.644 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H698 | Leishmania donovani | 100% | 100% |
A4HC45 | Leishmania braziliensis | 72% | 98% |
E9ACQ6 | Leishmania major | 94% | 100% |
E9AMJ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |