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: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 18 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
Related structures:
AlphaFold database: A0A3S7XBU6
Term | Name | Level | Count |
---|---|---|---|
GO:0038023 | signaling receptor activity | 2 | 3 |
GO:0060089 | molecular transducer activity | 1 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 108 | 112 | PF00656 | 0.730 |
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.606 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.488 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 199 | 201 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.513 |
DEG_ODPH_VHL_1 | 418 | 430 | PF01847 | 0.269 |
DEG_SPOP_SBC_1 | 125 | 129 | PF00917 | 0.646 |
DOC_CKS1_1 | 146 | 151 | PF01111 | 0.626 |
DOC_CKS1_1 | 175 | 180 | PF01111 | 0.648 |
DOC_CKS1_1 | 85 | 90 | PF01111 | 0.552 |
DOC_MAPK_DCC_7 | 36 | 45 | PF00069 | 0.598 |
DOC_MAPK_gen_1 | 16 | 22 | PF00069 | 0.639 |
DOC_MAPK_gen_1 | 34 | 42 | PF00069 | 0.577 |
DOC_MAPK_HePTP_8 | 403 | 415 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 36 | 45 | PF00069 | 0.598 |
DOC_MAPK_MEF2A_6 | 401 | 409 | PF00069 | 0.434 |
DOC_PP1_RVXF_1 | 345 | 351 | PF00149 | 0.469 |
DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.624 |
DOC_PP4_FxxP_1 | 361 | 364 | PF00568 | 0.391 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.205 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.694 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.654 |
LIG_14-3-3_CanoR_1 | 139 | 149 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 16 | 20 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 160 | 166 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 219 | 225 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 253 | 262 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 340 | 348 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 406 | 410 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 57 | 65 | PF00244 | 0.632 |
LIG_Actin_WH2_2 | 294 | 309 | PF00022 | 0.192 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.642 |
LIG_BRCT_BRCA1_1 | 38 | 42 | PF00533 | 0.619 |
LIG_deltaCOP1_diTrp_1 | 469 | 478 | PF00928 | 0.513 |
LIG_eIF4E_1 | 379 | 385 | PF01652 | 0.330 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.637 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.707 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.542 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.480 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.296 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.416 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.353 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.271 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.281 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.623 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.747 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.600 |
LIG_IBAR_NPY_1 | 245 | 247 | PF08397 | 0.506 |
LIG_LIR_Apic_2 | 164 | 168 | PF02991 | 0.621 |
LIG_LIR_Apic_2 | 359 | 364 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 129 | 140 | PF02991 | 0.630 |
LIG_LIR_Gen_1 | 18 | 26 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 281 | 290 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 39 | 50 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.717 |
LIG_LIR_Nem_3 | 18 | 22 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 240 | 244 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 281 | 285 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 75 | 79 | PF02991 | 0.621 |
LIG_NRBOX | 287 | 293 | PF00104 | 0.259 |
LIG_PCNA_yPIPBox_3 | 326 | 340 | PF02747 | 0.330 |
LIG_Pex14_1 | 395 | 399 | PF04695 | 0.330 |
LIG_REV1ctd_RIR_1 | 97 | 106 | PF16727 | 0.633 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.282 |
LIG_SH2_NCK_1 | 79 | 83 | PF00017 | 0.575 |
LIG_SH2_STAP1 | 187 | 191 | PF00017 | 0.613 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.164 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.282 |
LIG_SH2_STAT3 | 455 | 458 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.389 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.623 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.670 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.744 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.654 |
LIG_Sin3_3 | 382 | 389 | PF02671 | 0.249 |
LIG_SUMO_SIM_anti_2 | 381 | 388 | PF11976 | 0.330 |
LIG_SUMO_SIM_anti_2 | 424 | 429 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 381 | 388 | PF11976 | 0.332 |
LIG_TYR_ITIM | 291 | 296 | PF00017 | 0.330 |
LIG_WRC_WIRS_1 | 279 | 284 | PF05994 | 0.290 |
LIG_WRC_WIRS_1 | 358 | 363 | PF05994 | 0.368 |
LIG_WW_1 | 363 | 366 | PF00397 | 0.330 |
MOD_CDK_SPK_2 | 174 | 179 | PF00069 | 0.656 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.812 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.532 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.261 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.759 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.696 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.660 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.669 |
MOD_Cter_Amidation | 197 | 200 | PF01082 | 0.383 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.492 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.611 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.523 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.360 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.332 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.484 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.278 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.450 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.391 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.731 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.710 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.788 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.330 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.283 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.272 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.282 |
MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.337 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.409 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.638 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.463 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.330 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.318 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.164 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.350 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.515 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.403 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.286 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.362 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.332 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.485 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.355 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.341 |
MOD_NEK2_2 | 114 | 119 | PF00069 | 0.648 |
MOD_PIKK_1 | 103 | 109 | PF00454 | 0.657 |
MOD_PIKK_1 | 454 | 460 | PF00454 | 0.249 |
MOD_PKA_1 | 200 | 206 | PF00069 | 0.608 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.621 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.625 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.441 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.222 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.537 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.783 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.510 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.671 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.620 |
MOD_Plk_2-3 | 105 | 111 | PF00069 | 0.644 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.578 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.237 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.290 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.402 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.335 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.469 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.316 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.314 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.679 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.690 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.653 |
MOD_SUMO_for_1 | 101 | 104 | PF00179 | 0.632 |
TRG_DiLeu_BaEn_2 | 95 | 101 | PF01217 | 0.652 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 15 | 17 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 200 | 202 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.467 |
TRG_NLS_MonoExtN_4 | 196 | 203 | PF00514 | 0.573 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEB9 | Leptomonas seymouri | 50% | 94% |
A0A3S7XBT4 | Leishmania donovani | 37% | 100% |
A0A3S7XC05 | Leishmania donovani | 38% | 100% |
A4HQ64 | Leishmania braziliensis | 67% | 99% |
A4HQ67 | Leishmania braziliensis | 35% | 100% |
A4HQ68 | Leishmania braziliensis | 39% | 100% |
A4IDW4 | Leishmania infantum | 37% | 100% |
A4IDW5 | Leishmania infantum | 99% | 100% |
A4IDW6 | Leishmania infantum | 38% | 100% |
D0A451 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9ATY5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9ATY6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 98% |
E9ATY7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
Q07959 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 94% |
Q4Q0K9 | Leishmania major | 38% | 100% |
Q4Q0L0 | Leishmania major | 89% | 100% |
Q4Q0L1 | Leishmania major | 37% | 100% |
Q75F81 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 25% | 100% |