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. | yes | yes: 16 |
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. | yes | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | yes | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A0A3Q8IFS5
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0003723 | RNA binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 25 | 31 | PF00089 | 0.351 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.393 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.284 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.628 |
DEG_SCF_FBW7_1 | 110 | 115 | PF00400 | 0.593 |
DOC_CKS1_1 | 167 | 172 | PF01111 | 0.527 |
DOC_CKS1_1 | 56 | 61 | PF01111 | 0.351 |
DOC_MAPK_gen_1 | 341 | 347 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 42 | 50 | PF00069 | 0.354 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.663 |
DOC_PP4_FxxP_1 | 300 | 303 | PF00568 | 0.474 |
DOC_PP4_MxPP_1 | 212 | 215 | PF00568 | 0.537 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.446 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.351 |
LIG_14-3-3_CanoR_1 | 28 | 36 | PF00244 | 0.261 |
LIG_14-3-3_CanoR_1 | 383 | 393 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 43 | 49 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 448 | 457 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.351 |
LIG_AP2alpha_1 | 72 | 76 | PF02296 | 0.351 |
LIG_AP2alpha_2 | 219 | 221 | PF02296 | 0.565 |
LIG_EVH1_2 | 303 | 307 | PF00568 | 0.387 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.509 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.567 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.273 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.570 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.399 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.390 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.373 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.345 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.289 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.524 |
LIG_LIR_Apic_2 | 203 | 208 | PF02991 | 0.666 |
LIG_LIR_Gen_1 | 305 | 315 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 321 | 329 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 13 | 17 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.358 |
LIG_Pex14_2 | 72 | 76 | PF04695 | 0.351 |
LIG_SH2_GRB2like | 101 | 104 | PF00017 | 0.468 |
LIG_SH2_GRB2like | 438 | 441 | PF00017 | 0.452 |
LIG_SH2_SRC | 438 | 441 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 101 | 105 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 400 | 404 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.371 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.706 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.790 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.678 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.596 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.576 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.478 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.514 |
LIG_SUMO_SIM_anti_2 | 309 | 314 | PF11976 | 0.332 |
LIG_SUMO_SIM_anti_2 | 353 | 360 | PF11976 | 0.379 |
LIG_TRAF2_1 | 503 | 506 | PF00917 | 0.472 |
LIG_TRAF2_2 | 214 | 219 | PF00917 | 0.549 |
LIG_WRC_WIRS_1 | 358 | 363 | PF05994 | 0.384 |
MOD_CDK_SPxxK_3 | 406 | 413 | PF00069 | 0.400 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.366 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.294 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.430 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.505 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.553 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.567 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.352 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.405 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.568 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.512 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.202 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.423 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.525 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.387 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.377 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.339 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.383 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.606 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.577 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.530 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.292 |
MOD_NEK2_2 | 200 | 205 | PF00069 | 0.614 |
MOD_NEK2_2 | 318 | 323 | PF00069 | 0.306 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.582 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.766 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.261 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.519 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.286 |
MOD_Plk_2-3 | 453 | 459 | PF00069 | 0.458 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.688 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.391 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.359 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.441 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.389 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.264 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.653 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.562 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.434 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.412 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.351 |
MOD_SUMO_rev_2 | 477 | 484 | PF00179 | 0.466 |
MOD_SUMO_rev_2 | 494 | 504 | PF00179 | 0.602 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.626 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.818 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.357 |
TRG_Pf-PMV_PEXEL_1 | 469 | 473 | PF00026 | 0.422 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7M5 | Leptomonas seymouri | 64% | 100% |
A0A422N8U4 | Trypanosoma rangeli | 42% | 100% |
A4HK65 | Leishmania braziliensis | 82% | 100% |
A4I7Q0 | Leishmania infantum | 100% | 100% |
E9B2K9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 67% |
Q4Q5J8 | Leishmania major | 92% | 97% |
V5B118 | Trypanosoma cruzi | 43% | 100% |