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: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: Q4QHJ4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.345 |
CLV_PCSK_FUR_1 | 74 | 78 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.390 |
CLV_PCSK_PC1ET2_1 | 65 | 67 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.401 |
DEG_MDM2_SWIB_1 | 284 | 292 | PF02201 | 0.488 |
DOC_MAPK_gen_1 | 296 | 305 | PF00069 | 0.461 |
DOC_MAPK_gen_1 | 74 | 82 | PF00069 | 0.706 |
DOC_MAPK_MEF2A_6 | 298 | 307 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 394 | 402 | PF00069 | 0.543 |
DOC_MAPK_RevD_3 | 333 | 346 | PF00069 | 0.243 |
DOC_PP1_RVXF_1 | 296 | 303 | PF00149 | 0.461 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.293 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.248 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.227 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.650 |
DOC_USP7_UBL2_3 | 61 | 65 | PF12436 | 0.612 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.264 |
LIG_14-3-3_CanoR_1 | 24 | 30 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 348 | 353 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 355 | 359 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 4 | 13 | PF00244 | 0.648 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.726 |
LIG_BRCT_BRCA1_1 | 226 | 230 | PF00533 | 0.299 |
LIG_BRCT_BRCA1_1 | 400 | 404 | PF00533 | 0.359 |
LIG_BRCT_BRCA1_1 | 407 | 411 | PF00533 | 0.367 |
LIG_EH1_1 | 372 | 380 | PF00400 | 0.259 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.583 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.565 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.292 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.370 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.353 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.573 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.587 |
LIG_LIR_Apic_2 | 356 | 361 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 234 | 242 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 377 | 387 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 395 | 404 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 414 | 421 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 437 | 447 | PF02991 | 0.304 |
LIG_LIR_LC3C_4 | 234 | 239 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 234 | 238 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 377 | 383 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 414 | 419 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 441 | 447 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 465 | 470 | PF02991 | 0.311 |
LIG_MLH1_MIPbox_1 | 226 | 230 | PF16413 | 0.228 |
LIG_Pex14_1 | 324 | 328 | PF04695 | 0.300 |
LIG_Pex14_2 | 221 | 225 | PF04695 | 0.295 |
LIG_Pex14_2 | 284 | 288 | PF04695 | 0.468 |
LIG_SH2_CRK | 129 | 133 | PF00017 | 0.353 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.305 |
LIG_SH2_CRK | 444 | 448 | PF00017 | 0.356 |
LIG_SH2_PTP2 | 304 | 307 | PF00017 | 0.293 |
LIG_SH2_PTP2 | 397 | 400 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 226 | 230 | PF00017 | 0.267 |
LIG_SH2_STAP1 | 406 | 410 | PF00017 | 0.438 |
LIG_SH2_STAT3 | 181 | 184 | PF00017 | 0.261 |
LIG_SH2_STAT3 | 393 | 396 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.227 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.541 |
LIG_SUMO_SIM_anti_2 | 477 | 483 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 417 | 422 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 78 | 83 | PF11976 | 0.555 |
LIG_TRAF2_1 | 14 | 17 | PF00917 | 0.700 |
LIG_TYR_ITIM | 127 | 132 | PF00017 | 0.353 |
LIG_WRC_WIRS_1 | 198 | 203 | PF05994 | 0.354 |
LIG_WRC_WIRS_1 | 222 | 227 | PF05994 | 0.353 |
LIG_WRC_WIRS_1 | 242 | 247 | PF05994 | 0.183 |
LIG_WRC_WIRS_1 | 349 | 354 | PF05994 | 0.304 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.571 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.399 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.318 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.627 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.339 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.245 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.251 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.832 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.575 |
MOD_CK2_1 | 459 | 465 | PF00069 | 0.302 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.593 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.771 |
MOD_Cter_Amidation | 154 | 157 | PF01082 | 0.496 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.443 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.622 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.359 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.479 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.459 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.534 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.576 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.533 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.701 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.731 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.348 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.489 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.295 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.378 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.347 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.378 |
MOD_LATS_1 | 47 | 53 | PF00433 | 0.550 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.461 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.471 |
MOD_N-GLC_1 | 456 | 461 | PF02516 | 0.434 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.340 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.470 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.335 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.216 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.468 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.380 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.388 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.466 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.502 |
MOD_NEK2_2 | 308 | 313 | PF00069 | 0.254 |
MOD_OFUCOSY | 139 | 145 | PF10250 | 0.215 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.575 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.443 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.669 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.234 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.699 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.324 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.352 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.646 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.270 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.314 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.627 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.361 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.370 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.472 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.350 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.414 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.324 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.256 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.377 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.349 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.360 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.677 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.264 |
TRG_DiLeu_BaEn_1 | 465 | 470 | PF01217 | 0.353 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.304 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 34 | 36 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.534 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6X2 | Leptomonas seymouri | 63% | 97% |
A0A0N1PC74 | Leptomonas seymouri | 26% | 97% |
A0A0N1PCA2 | Leptomonas seymouri | 29% | 100% |
A0A3Q8I8Q6 | Leishmania donovani | 92% | 100% |
A0A3S7WR28 | Leishmania donovani | 27% | 100% |
A0A3S7X1E1 | Leishmania donovani | 27% | 94% |
A4H605 | Leishmania braziliensis | 70% | 96% |
A4H606 | Leishmania braziliensis | 26% | 100% |
A4HGF8 | Leishmania braziliensis | 29% | 94% |
A4HUD2 | Leishmania infantum | 92% | 100% |
A4HUD3 | Leishmania infantum | 27% | 100% |
A4I3I9 | Leishmania infantum | 28% | 94% |
E9AN32 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9AN33 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AZT1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 94% |
Q4Q8F3 | Leishmania major | 28% | 100% |
Q4QHJ3 | Leishmania major | 27% | 97% |