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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
Related structures:
AlphaFold database: A4HIW8
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0008643 | carbohydrate transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.423 |
CLV_PCSK_FUR_1 | 161 | 165 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 163 | 165 | PF00082 | 0.371 |
CLV_PCSK_PC1ET2_1 | 297 | 299 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.255 |
DEG_APCC_DBOX_1 | 101 | 109 | PF00400 | 0.275 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.578 |
DEG_MDM2_SWIB_1 | 433 | 440 | PF02201 | 0.273 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.599 |
DOC_CDC14_PxL_1 | 92 | 100 | PF14671 | 0.399 |
DOC_CKS1_1 | 477 | 482 | PF01111 | 0.452 |
DOC_MAPK_gen_1 | 163 | 173 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 411 | 420 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 5 | 11 | PF00069 | 0.584 |
DOC_MAPK_gen_1 | 544 | 553 | PF00069 | 0.588 |
DOC_MAPK_MEF2A_6 | 164 | 173 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 414 | 422 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 446 | 455 | PF00069 | 0.330 |
DOC_MAPK_MEF2A_6 | 465 | 474 | PF00069 | 0.328 |
DOC_PP2B_PxIxI_1 | 168 | 174 | PF00149 | 0.481 |
DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.559 |
DOC_PP4_FxxP_1 | 351 | 354 | PF00568 | 0.312 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 508 | 512 | PF00917 | 0.392 |
DOC_USP7_UBL2_3 | 446 | 450 | PF12436 | 0.310 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.620 |
LIG_14-3-3_CanoR_1 | 137 | 143 | PF00244 | 0.204 |
LIG_14-3-3_CanoR_1 | 298 | 307 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 310 | 314 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 319 | 323 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 361 | 365 | PF00244 | 0.286 |
LIG_Actin_WH2_2 | 451 | 467 | PF00022 | 0.289 |
LIG_APCC_ABBA_1 | 329 | 334 | PF00400 | 0.535 |
LIG_eIF4E_1 | 521 | 527 | PF01652 | 0.234 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.313 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.546 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.436 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.382 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.542 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.316 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.445 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.613 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.663 |
LIG_LIR_Gen_1 | 121 | 129 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 141 | 152 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 343 | 354 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 80 | 90 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 432 | 436 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 485 | 491 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 519 | 525 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 80 | 85 | PF02991 | 0.538 |
LIG_MYND_1 | 96 | 100 | PF01753 | 0.206 |
LIG_NRBOX | 385 | 391 | PF00104 | 0.312 |
LIG_Pex14_1 | 77 | 81 | PF04695 | 0.587 |
LIG_Pex14_2 | 17 | 21 | PF04695 | 0.537 |
LIG_Pex14_2 | 336 | 340 | PF04695 | 0.410 |
LIG_Pex14_2 | 342 | 346 | PF04695 | 0.350 |
LIG_Pex14_2 | 364 | 368 | PF04695 | 0.301 |
LIG_Pex14_2 | 430 | 434 | PF04695 | 0.283 |
LIG_PTB_Apo_2 | 356 | 363 | PF02174 | 0.448 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.312 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.271 |
LIG_SH2_CRK | 264 | 268 | PF00017 | 0.322 |
LIG_SH2_NCK_1 | 483 | 487 | PF00017 | 0.507 |
LIG_SH2_STAP1 | 140 | 144 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 195 | 199 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 395 | 399 | PF00017 | 0.281 |
LIG_SH2_STAP1 | 483 | 487 | PF00017 | 0.507 |
LIG_SH2_STAT3 | 400 | 403 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.572 |
LIG_SH3_1 | 264 | 270 | PF00018 | 0.327 |
LIG_SH3_2 | 41 | 46 | PF14604 | 0.640 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.518 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.341 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.603 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.629 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.369 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.352 |
LIG_SUMO_SIM_anti_2 | 196 | 203 | PF11976 | 0.247 |
LIG_TRAF2_1 | 561 | 564 | PF00917 | 0.679 |
LIG_TYR_ITIM | 142 | 147 | PF00017 | 0.373 |
LIG_TYR_ITSM | 300 | 307 | PF00017 | 0.486 |
LIG_UBA3_1 | 155 | 163 | PF00899 | 0.303 |
LIG_UBA3_1 | 289 | 297 | PF00899 | 0.274 |
LIG_UBA3_1 | 525 | 532 | PF00899 | 0.239 |
LIG_WRC_WIRS_1 | 120 | 125 | PF05994 | 0.345 |
LIG_WRC_WIRS_1 | 430 | 435 | PF05994 | 0.369 |
LIG_WW_3 | 39 | 43 | PF00397 | 0.682 |
MOD_CDC14_SPxK_1 | 330 | 333 | PF00782 | 0.538 |
MOD_CDK_SPK_2 | 476 | 481 | PF00069 | 0.443 |
MOD_CDK_SPxK_1 | 327 | 333 | PF00069 | 0.535 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.410 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.400 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.604 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.289 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.328 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.299 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.577 |
MOD_CK2_1 | 557 | 563 | PF00069 | 0.747 |
MOD_GlcNHglycan | 233 | 237 | PF01048 | 0.349 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.490 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.340 |
MOD_GlcNHglycan | 47 | 52 | PF01048 | 0.459 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.371 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.385 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.356 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.578 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.446 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.608 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.252 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.361 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.313 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.493 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.303 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.309 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.590 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.319 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.494 |
MOD_N-GLC_1 | 557 | 562 | PF02516 | 0.417 |
MOD_N-GLC_2 | 461 | 463 | PF02516 | 0.213 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.305 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.449 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.410 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.531 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.430 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.379 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.358 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.295 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.490 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.560 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.357 |
MOD_NEK2_2 | 429 | 434 | PF00069 | 0.301 |
MOD_NEK2_2 | 454 | 459 | PF00069 | 0.305 |
MOD_PIKK_1 | 110 | 116 | PF00454 | 0.304 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.269 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.643 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.552 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.290 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.297 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.665 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.381 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.306 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.404 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.275 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.497 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.298 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.609 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.530 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.629 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.449 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.619 |
MOD_SUMO_for_1 | 162 | 165 | PF00179 | 0.485 |
TRG_DiLeu_BaLyEn_6 | 414 | 419 | PF01217 | 0.404 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.339 |
TRG_ER_diArg_1 | 304 | 306 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.623 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYC7 | Leptomonas seymouri | 57% | 100% |
A0A0N1I3H1 | Leptomonas seymouri | 29% | 85% |
A0A3Q8IF44 | Leishmania donovani | 81% | 100% |
A0A3Q8ILR5 | Leishmania donovani | 26% | 100% |
A4HL09 | Leishmania braziliensis | 27% | 100% |
A4I8J0 | Leishmania infantum | 26% | 100% |
E9AHK6 | Leishmania infantum | 81% | 100% |
E9B1F2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E9B3F0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4Q4Q0 | Leishmania major | 25% | 98% |
Q4Q6R0 | Leishmania major | 77% | 100% |