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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4QCK8
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 11 |
GO:0022857 | transmembrane transporter activity | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.528 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.347 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.362 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.519 |
DOC_CDC14_PxL_1 | 258 | 266 | PF14671 | 0.387 |
DOC_CYCLIN_RxL_1 | 139 | 151 | PF00134 | 0.364 |
DOC_CYCLIN_RxL_1 | 263 | 274 | PF00134 | 0.341 |
DOC_CYCLIN_RxL_1 | 56 | 67 | PF00134 | 0.554 |
DOC_MAPK_gen_1 | 105 | 112 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 410 | 418 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 105 | 114 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 170 | 178 | PF00069 | 0.519 |
DOC_PP1_RVXF_1 | 264 | 271 | PF00149 | 0.341 |
DOC_PP1_RVXF_1 | 411 | 418 | PF00149 | 0.461 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.548 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.314 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 239 | 249 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 41 | 47 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 533 | 539 | PF00244 | 0.538 |
LIG_Actin_WH2_2 | 160 | 177 | PF00022 | 0.334 |
LIG_APCC_ABBA_1 | 366 | 371 | PF00400 | 0.387 |
LIG_BRCT_BRCA1_1 | 358 | 362 | PF00533 | 0.361 |
LIG_BRCT_BRCA1_1 | 377 | 381 | PF00533 | 0.176 |
LIG_BRCT_BRCA1_1 | 447 | 451 | PF00533 | 0.225 |
LIG_BRCT_BRCA1_1 | 503 | 507 | PF00533 | 0.398 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.502 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.341 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.334 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.492 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.305 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.316 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.558 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.492 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.357 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.426 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.334 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.426 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.446 |
LIG_LIR_Apic_2 | 230 | 236 | PF02991 | 0.357 |
LIG_LIR_Apic_2 | 32 | 37 | PF02991 | 0.517 |
LIG_LIR_Apic_2 | 341 | 346 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 13 | 21 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 255 | 264 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 269 | 278 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 286 | 297 | PF02991 | 0.264 |
LIG_LIR_Gen_1 | 363 | 373 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 448 | 456 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 98 | 104 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 150 | 155 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 160 | 164 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 201 | 206 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 269 | 273 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 274 | 279 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 363 | 368 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 371 | 376 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 378 | 384 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 386 | 391 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 448 | 452 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 537 | 541 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.611 |
LIG_MLH1_MIPbox_1 | 503 | 507 | PF16413 | 0.398 |
LIG_OCRL_FandH_1 | 102 | 114 | PF00620 | 0.425 |
LIG_PDZ_Class_3 | 545 | 550 | PF00595 | 0.608 |
LIG_Pex14_1 | 34 | 38 | PF04695 | 0.522 |
LIG_Pex14_1 | 365 | 369 | PF04695 | 0.314 |
LIG_Pex14_2 | 157 | 161 | PF04695 | 0.334 |
LIG_Pex14_2 | 99 | 103 | PF04695 | 0.584 |
LIG_PTB_Apo_2 | 424 | 431 | PF02174 | 0.334 |
LIG_SH2_CRK | 171 | 175 | PF00017 | 0.541 |
LIG_SH2_CRK | 500 | 504 | PF00017 | 0.314 |
LIG_SH2_NCK_1 | 469 | 473 | PF00017 | 0.461 |
LIG_SH2_PTP2 | 15 | 18 | PF00017 | 0.504 |
LIG_SH2_PTP2 | 258 | 261 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 373 | 377 | PF00017 | 0.296 |
LIG_SH2_STAP1 | 469 | 473 | PF00017 | 0.461 |
LIG_SH2_STAT3 | 541 | 544 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.553 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.314 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.413 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.521 |
LIG_SUMO_SIM_anti_2 | 331 | 337 | PF11976 | 0.542 |
LIG_SxIP_EBH_1 | 155 | 166 | PF03271 | 0.342 |
LIG_TRAF2_1 | 478 | 481 | PF00917 | 0.541 |
LIG_TYR_ITIM | 256 | 261 | PF00017 | 0.314 |
LIG_TYR_ITIM | 353 | 358 | PF00017 | 0.420 |
LIG_TYR_ITIM | 467 | 472 | PF00017 | 0.314 |
LIG_TYR_ITIM | 498 | 503 | PF00017 | 0.357 |
LIG_WRC_WIRS_1 | 158 | 163 | PF05994 | 0.342 |
LIG_WRC_WIRS_1 | 384 | 389 | PF05994 | 0.334 |
MOD_CDK_SPxxK_3 | 431 | 438 | PF00069 | 0.426 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.314 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.459 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.398 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.202 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.312 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.436 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.413 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.392 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.314 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.314 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.357 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.314 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.421 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.424 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.206 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.352 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.364 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.314 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.349 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.377 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.314 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.349 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.294 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.370 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.267 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.299 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.334 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.304 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.435 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.418 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.316 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.379 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.428 |
MOD_N-GLC_1 | 534 | 539 | PF02516 | 0.399 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.377 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.387 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.390 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.155 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.376 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.438 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.356 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.349 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.438 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.438 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.360 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.336 |
MOD_NEK2_2 | 364 | 369 | PF00069 | 0.327 |
MOD_NEK2_2 | 383 | 388 | PF00069 | 0.314 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.426 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.436 |
MOD_PKA_1 | 266 | 272 | PF00069 | 0.459 |
MOD_PKA_1 | 47 | 53 | PF00069 | 0.435 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.314 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.403 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.428 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.448 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.372 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.445 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.255 |
MOD_Plk_1 | 436 | 442 | PF00069 | 0.426 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.314 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.403 |
MOD_Plk_2-3 | 318 | 324 | PF00069 | 0.407 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.342 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.426 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.334 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.362 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.385 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.235 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.357 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.357 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.314 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.426 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.443 |
MOD_SUMO_rev_2 | 314 | 321 | PF00179 | 0.370 |
TRG_DiLeu_BaEn_1 | 331 | 336 | PF01217 | 0.387 |
TRG_DiLeu_BaEn_3 | 379 | 385 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.182 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 500 | 503 | PF00928 | 0.314 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJH4 | Leptomonas seymouri | 80% | 100% |
A0A0N1ILZ7 | Leptomonas seymouri | 22% | 100% |
A0A0S4J692 | Bodo saltans | 23% | 91% |
A0A0S4J989 | Bodo saltans | 50% | 100% |
A0A1X0NWR8 | Trypanosomatidae | 24% | 100% |
A0A1X0NXK8 | Trypanosomatidae | 65% | 100% |
A0A3R7NE20 | Trypanosoma rangeli | 61% | 100% |
A0A3S7WUW1 | Leishmania donovani | 23% | 100% |
A0A3S7WW86 | Leishmania donovani | 96% | 100% |
A4H9A1 | Leishmania braziliensis | 23% | 100% |
A4HBK5 | Leishmania braziliensis | 89% | 100% |
A4HXM1 | Leishmania infantum | 23% | 100% |
B2RXV4 | Mus musculus | 23% | 98% |
E9AGU5 | Leishmania infantum | 96% | 100% |
E9ARB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9AUX4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
O01735 | Caenorhabditis elegans | 24% | 94% |
P60815 | Rattus norvegicus | 22% | 100% |
Q4QE46 | Leishmania major | 24% | 100% |
Q66H95 | Rattus norvegicus | 22% | 100% |
Q6GNV7 | Xenopus laevis | 22% | 100% |
Q6UXD7 | Homo sapiens | 24% | 98% |
Q8BFQ6 | Mus musculus | 22% | 100% |
Q91X85 | Mus musculus | 22% | 100% |
Q96SL1 | Homo sapiens | 22% | 100% |
Q9ES43 | Mus terricolor | 23% | 98% |
Q9N1F2 | Felis catus | 22% | 98% |
Q9UPI3 | Homo sapiens | 21% | 100% |
Q9Y5Y0 | Homo sapiens | 23% | 99% |
V5BQV3 | Trypanosoma cruzi | 24% | 100% |
V5DGX2 | Trypanosoma cruzi | 60% | 100% |