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: A4HNT4
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 | 252 | 256 | PF00656 | 0.633 |
CLV_C14_Caspase3-7 | 354 | 358 | PF00656 | 0.434 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.468 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 465 | 467 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.388 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.520 |
DOC_CDC14_PxL_1 | 410 | 418 | PF14671 | 0.426 |
DOC_CKS1_1 | 105 | 110 | PF01111 | 0.545 |
DOC_MAPK_gen_1 | 196 | 203 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 265 | 275 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 196 | 203 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 265 | 273 | PF00069 | 0.383 |
DOC_MAPK_MEF2A_6 | 415 | 424 | PF00069 | 0.401 |
DOC_MAPK_NFAT4_5 | 268 | 276 | PF00069 | 0.398 |
DOC_MAPK_RevD_3 | 488 | 501 | PF00069 | 0.422 |
DOC_PP2B_LxvP_1 | 365 | 368 | PF13499 | 0.423 |
DOC_PP4_FxxP_1 | 275 | 278 | PF00568 | 0.404 |
DOC_PP4_MxPP_1 | 106 | 109 | PF00568 | 0.539 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.678 |
DOC_USP7_UBL2_3 | 261 | 265 | PF12436 | 0.477 |
DOC_USP7_UBL2_3 | 305 | 309 | PF12436 | 0.451 |
DOC_USP7_UBL2_3 | 360 | 364 | PF12436 | 0.462 |
DOC_USP7_UBL2_3 | 448 | 452 | PF12436 | 0.411 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.507 |
LIG_14-3-3_CanoR_1 | 205 | 211 | PF00244 | 0.489 |
LIG_APCC_ABBA_1 | 349 | 354 | PF00400 | 0.430 |
LIG_BRCT_BRCA1_1 | 483 | 487 | PF00533 | 0.396 |
LIG_eIF4E_1 | 436 | 442 | PF01652 | 0.439 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.479 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.442 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.438 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.391 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.558 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.465 |
LIG_FHA_2 | 491 | 497 | PF00498 | 0.424 |
LIG_LIR_Apic_2 | 274 | 278 | PF02991 | 0.405 |
LIG_LIR_Apic_2 | 296 | 300 | PF02991 | 0.510 |
LIG_LIR_Apic_2 | 329 | 335 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 345 | 352 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 484 | 492 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 431 | 436 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 484 | 490 | PF02991 | 0.377 |
LIG_LYPXL_yS_3 | 57 | 60 | PF13949 | 0.538 |
LIG_PDZ_Class_1 | 523 | 528 | PF00595 | 0.500 |
LIG_Pex14_2 | 359 | 363 | PF04695 | 0.396 |
LIG_PTB_Apo_2 | 162 | 169 | PF02174 | 0.580 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.414 |
LIG_SH2_CRK | 87 | 91 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 207 | 211 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 454 | 458 | PF00017 | 0.626 |
LIG_SH2_STAT3 | 119 | 122 | PF00017 | 0.650 |
LIG_SH2_STAT3 | 155 | 158 | PF00017 | 0.705 |
LIG_SH2_STAT3 | 169 | 172 | PF00017 | 0.506 |
LIG_SH2_STAT3 | 450 | 453 | PF00017 | 0.409 |
LIG_SH2_STAT3 | 46 | 49 | PF00017 | 0.703 |
LIG_SH2_STAT3 | 78 | 81 | PF00017 | 0.593 |
LIG_SH2_STAT3 | 89 | 92 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.615 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.612 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.456 |
LIG_TRAF2_1 | 493 | 496 | PF00917 | 0.476 |
LIG_TYR_ITIM | 55 | 60 | PF00017 | 0.538 |
LIG_TYR_ITSM | 327 | 334 | PF00017 | 0.372 |
MOD_CDK_SPK_2 | 274 | 279 | PF00069 | 0.413 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.568 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.567 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.330 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.362 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.487 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.470 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.649 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.642 |
MOD_CK2_1 | 490 | 496 | PF00069 | 0.428 |
MOD_Cter_Amidation | 310 | 313 | PF01082 | 0.435 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.677 |
MOD_GlcNHglycan | 255 | 259 | PF01048 | 0.535 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.475 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.292 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.349 |
MOD_GlcNHglycan | 396 | 400 | PF01048 | 0.448 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.607 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.632 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.600 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.357 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.482 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.671 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.539 |
MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.532 |
MOD_N-GLC_1 | 399 | 404 | PF02516 | 0.413 |
MOD_N-GLC_2 | 129 | 131 | PF02516 | 0.563 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.535 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.423 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.485 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.352 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.387 |
MOD_NEK2_2 | 335 | 340 | PF00069 | 0.362 |
MOD_OFUCOSY | 479 | 485 | PF10250 | 0.373 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.686 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.747 |
MOD_PK_1 | 197 | 203 | PF00069 | 0.412 |
MOD_PKA_1 | 500 | 506 | PF00069 | 0.396 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.538 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.585 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.418 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.412 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.401 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.723 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.557 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.622 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.426 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.360 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.378 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.597 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.497 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.330 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.534 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.503 |
MOD_SUMO_rev_2 | 234 | 241 | PF00179 | 0.676 |
MOD_SUMO_rev_2 | 257 | 267 | PF00179 | 0.576 |
MOD_SUMO_rev_2 | 306 | 314 | PF00179 | 0.473 |
MOD_SUMO_rev_2 | 494 | 503 | PF00179 | 0.462 |
TRG_DiLeu_BaEn_2 | 482 | 488 | PF01217 | 0.381 |
TRG_ENDOCYTIC_2 | 207 | 210 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.538 |
TRG_ER_diArg_1 | 464 | 467 | PF00400 | 0.444 |
TRG_NES_CRM1_1 | 382 | 396 | PF08389 | 0.317 |
TRG_NLS_MonoExtN_4 | 462 | 468 | PF00514 | 0.436 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7W2 | Leptomonas seymouri | 67% | 100% |
A0A3S7XAD2 | Leishmania donovani | 84% | 97% |
A4ICR0 | Leishmania infantum | 84% | 97% |
E9ASJ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 98% |
Q4Q202 | Leishmania major | 84% | 100% |