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: 4 |
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9ASJ4
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 258 | 262 | PF00656 | 0.613 |
CLV_C14_Caspase3-7 | 360 | 364 | PF00656 | 0.438 |
CLV_C14_Caspase3-7 | 505 | 509 | PF00656 | 0.487 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.464 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.422 |
CLV_PCSK_PC1ET2_1 | 471 | 473 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.548 |
DOC_CDC14_PxL_1 | 416 | 424 | PF14671 | 0.409 |
DOC_MAPK_gen_1 | 202 | 209 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 271 | 281 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 202 | 209 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 271 | 279 | PF00069 | 0.374 |
DOC_MAPK_MEF2A_6 | 421 | 430 | PF00069 | 0.391 |
DOC_MAPK_NFAT4_5 | 274 | 282 | PF00069 | 0.388 |
DOC_MAPK_RevD_3 | 494 | 507 | PF00069 | 0.417 |
DOC_PP2B_LxvP_1 | 371 | 374 | PF13499 | 0.420 |
DOC_PP4_FxxP_1 | 281 | 284 | PF00568 | 0.389 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.615 |
DOC_USP7_UBL2_3 | 267 | 271 | PF12436 | 0.475 |
DOC_USP7_UBL2_3 | 311 | 315 | PF12436 | 0.446 |
DOC_USP7_UBL2_3 | 366 | 370 | PF12436 | 0.456 |
DOC_USP7_UBL2_3 | 454 | 458 | PF12436 | 0.407 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 211 | 217 | PF00244 | 0.464 |
LIG_APCC_ABBA_1 | 355 | 360 | PF00400 | 0.430 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.400 |
LIG_BRCT_BRCA1_1 | 489 | 493 | PF00533 | 0.396 |
LIG_eIF4E_1 | 442 | 448 | PF01652 | 0.436 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.475 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.437 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.430 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.384 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.531 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.459 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.417 |
LIG_FHA_2 | 516 | 522 | PF00498 | 0.490 |
LIG_LIR_Apic_2 | 280 | 284 | PF02991 | 0.390 |
LIG_LIR_Apic_2 | 302 | 306 | PF02991 | 0.507 |
LIG_LIR_Apic_2 | 335 | 341 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 351 | 358 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 490 | 498 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 437 | 442 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 490 | 496 | PF02991 | 0.377 |
LIG_Pex14_2 | 365 | 369 | PF04695 | 0.390 |
LIG_PTB_Apo_2 | 168 | 175 | PF02174 | 0.569 |
LIG_SH2_CRK | 338 | 342 | PF00017 | 0.410 |
LIG_SH2_GRB2like | 354 | 357 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 213 | 217 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 460 | 464 | PF00017 | 0.622 |
LIG_SH2_STAT3 | 125 | 128 | PF00017 | 0.635 |
LIG_SH2_STAT3 | 161 | 164 | PF00017 | 0.693 |
LIG_SH2_STAT3 | 175 | 178 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 456 | 459 | PF00017 | 0.405 |
LIG_SH2_STAT3 | 52 | 55 | PF00017 | 0.691 |
LIG_SH2_STAT3 | 84 | 87 | PF00017 | 0.583 |
LIG_SH2_STAT3 | 95 | 98 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.635 |
LIG_SH3_2 | 119 | 124 | PF14604 | 0.630 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.641 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.572 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.438 |
LIG_TRAF2_1 | 499 | 502 | PF00917 | 0.468 |
LIG_TRAF2_1 | 518 | 521 | PF00917 | 0.417 |
LIG_TYR_ITSM | 333 | 340 | PF00017 | 0.369 |
LIG_UBA3_1 | 204 | 208 | PF00899 | 0.369 |
MOD_CDK_SPK_2 | 280 | 285 | PF00069 | 0.398 |
MOD_CDK_SPxxK_3 | 260 | 267 | PF00069 | 0.521 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.636 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.549 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.312 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.479 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.466 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.648 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.650 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.581 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.418 |
MOD_CK2_1 | 515 | 521 | PF00069 | 0.566 |
MOD_Cter_Amidation | 316 | 319 | PF01082 | 0.425 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.666 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.662 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.508 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.452 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.408 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.288 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.345 |
MOD_GlcNHglycan | 402 | 406 | PF01048 | 0.446 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.608 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.609 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.616 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.538 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.353 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.480 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.504 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.652 |
MOD_N-GLC_1 | 405 | 410 | PF02516 | 0.403 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.412 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.463 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.350 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.382 |
MOD_NEK2_2 | 341 | 346 | PF00069 | 0.357 |
MOD_NEK2_2 | 424 | 429 | PF00069 | 0.421 |
MOD_OFUCOSY | 485 | 491 | PF10250 | 0.369 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.669 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.727 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.735 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.533 |
MOD_PK_1 | 203 | 209 | PF00069 | 0.401 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.416 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.400 |
MOD_Plk_1 | 424 | 430 | PF00069 | 0.394 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.703 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.607 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.414 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.355 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.514 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.526 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.312 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.502 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.634 |
MOD_SUMO_for_1 | 313 | 316 | PF00179 | 0.452 |
MOD_SUMO_for_1 | 537 | 540 | PF00179 | 0.470 |
MOD_SUMO_rev_2 | 240 | 247 | PF00179 | 0.657 |
MOD_SUMO_rev_2 | 263 | 273 | PF00179 | 0.562 |
MOD_SUMO_rev_2 | 312 | 320 | PF00179 | 0.467 |
MOD_SUMO_rev_2 | 500 | 509 | PF00179 | 0.456 |
TRG_DiLeu_BaEn_2 | 488 | 494 | PF01217 | 0.380 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 470 | 473 | PF00400 | 0.440 |
TRG_NLS_MonoExtN_4 | 468 | 474 | PF00514 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7W2 | Leptomonas seymouri | 69% | 100% |
A0A3S7XAD2 | Leishmania donovani | 93% | 100% |
A4HNT4 | Leishmania braziliensis | 85% | 100% |
A4ICR0 | Leishmania infantum | 93% | 99% |
Q4Q202 | Leishmania major | 94% | 100% |