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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AZZ1
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006869 | lipid transport | 5 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0008289 | lipid binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 415 | 419 | PF00656 | 0.662 |
CLV_MEL_PAP_1 | 341 | 347 | PF00089 | 0.514 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.449 |
DEG_APCC_DBOX_1 | 343 | 351 | PF00400 | 0.439 |
DEG_SCF_FBW7_1 | 80 | 87 | PF00400 | 0.553 |
DEG_SPOP_SBC_1 | 203 | 207 | PF00917 | 0.512 |
DEG_SPOP_SBC_1 | 285 | 289 | PF00917 | 0.622 |
DEG_SPOP_SBC_1 | 29 | 33 | PF00917 | 0.479 |
DOC_MAPK_MEF2A_6 | 134 | 143 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 337 | 345 | PF00069 | 0.467 |
DOC_PP1_RVXF_1 | 143 | 149 | PF00149 | 0.519 |
DOC_PP2B_LxvP_1 | 451 | 454 | PF13499 | 0.470 |
DOC_SPAK_OSR1_1 | 315 | 319 | PF12202 | 0.449 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.626 |
DOC_USP7_MATH_2 | 62 | 68 | PF00917 | 0.669 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.648 |
LIG_14-3-3_CanoR_1 | 315 | 321 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 344 | 348 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 458 | 464 | PF00244 | 0.534 |
LIG_Actin_WH2_2 | 329 | 346 | PF00022 | 0.515 |
LIG_Actin_WH2_2 | 432 | 450 | PF00022 | 0.471 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 403 | 407 | PF00533 | 0.642 |
LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.675 |
LIG_deltaCOP1_diTrp_1 | 147 | 154 | PF00928 | 0.407 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.497 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.689 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.600 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.324 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.579 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.639 |
LIG_IRF3_LxIS_1 | 25 | 31 | PF10401 | 0.481 |
LIG_LIR_Apic_2 | 372 | 377 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 151 | 160 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 359 | 366 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 405 | 416 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 405 | 411 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 87 | 91 | PF02991 | 0.589 |
LIG_PCNA_yPIPBox_3 | 355 | 367 | PF02747 | 0.430 |
LIG_Pex14_2 | 407 | 411 | PF04695 | 0.614 |
LIG_SH2_GRB2like | 429 | 432 | PF00017 | 0.562 |
LIG_SH2_PTP2 | 361 | 364 | PF00017 | 0.370 |
LIG_SH2_SRC | 140 | 143 | PF00017 | 0.567 |
LIG_SH2_STAT3 | 280 | 283 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.712 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.562 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.391 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.619 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.495 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.429 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.487 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.440 |
LIG_TYR_ITIM | 138 | 143 | PF00017 | 0.572 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.625 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.647 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.662 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.690 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.629 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.624 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.749 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.416 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.656 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.646 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.813 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.654 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.646 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.613 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.695 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.765 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.749 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.747 |
MOD_GlcNHglycan | 423 | 428 | PF01048 | 0.757 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.654 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.819 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.659 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.715 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.636 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.598 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.640 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.606 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.756 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.260 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.701 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.592 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.528 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.776 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.749 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.613 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.621 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.587 |
MOD_N-GLC_2 | 369 | 371 | PF02516 | 0.366 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.741 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.660 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.363 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.387 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.444 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.588 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.641 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.523 |
MOD_NEK2_2 | 320 | 325 | PF00069 | 0.273 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.748 |
MOD_PIKK_1 | 433 | 439 | PF00454 | 0.423 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.737 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.503 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.421 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.484 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.465 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.732 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.521 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.486 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.623 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.485 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.700 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.544 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.618 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.667 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.450 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.646 |
TRG_DiLeu_BaEn_2 | 433 | 439 | PF01217 | 0.483 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.613 |
TRG_ER_diArg_1 | 387 | 390 | PF00400 | 0.385 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P822 | Leptomonas seymouri | 57% | 75% |
A0A3S7X1N8 | Leishmania donovani | 85% | 75% |
A4HGM5 | Leishmania braziliensis | 72% | 100% |
A4I3P9 | Leishmania infantum | 85% | 100% |
D0A8B3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
Q4Q894 | Leishmania major | 89% | 99% |
V5DBB8 | Trypanosoma cruzi | 28% | 100% |