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:0005789 | endoplasmic reticulum membrane | 4 | 2 |
GO:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 9 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0044232 | organelle membrane contact site | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0140268 | endoplasmic reticulum-plasma membrane contact site | 3 | 2 |
Related structures:
AlphaFold database: Q4QEC5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006869 | lipid transport | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015850 | organic hydroxy compound transport | 5 | 2 |
GO:0015918 | sterol transport | 6 | 2 |
GO:0032365 | intracellular lipid transport | 4 | 2 |
GO:0032366 | intracellular sterol transport | 5 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 2 |
GO:0005319 | lipid transporter activity | 2 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005496 | steroid binding | 3 | 2 |
GO:0008289 | lipid binding | 2 | 2 |
GO:0015248 | sterol transporter activity | 3 | 2 |
GO:0032934 | sterol binding | 4 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0120013 | lipid transfer activity | 3 | 2 |
GO:0120015 | sterol transfer activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.572 |
CLV_C14_Caspase3-7 | 217 | 221 | PF00656 | 0.342 |
CLV_C14_Caspase3-7 | 525 | 529 | PF00656 | 0.385 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.772 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 559 | 561 | PF00675 | 0.777 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.725 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.706 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.467 |
DEG_APCC_DBOX_1 | 448 | 456 | PF00400 | 0.342 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.340 |
DOC_CDC14_PxL_1 | 455 | 463 | PF14671 | 0.217 |
DOC_CKS1_1 | 162 | 167 | PF01111 | 0.509 |
DOC_CKS1_1 | 2 | 7 | PF01111 | 0.401 |
DOC_CKS1_1 | 369 | 374 | PF01111 | 0.407 |
DOC_CYCLIN_yCln2_LP_2 | 369 | 375 | PF00134 | 0.292 |
DOC_CYCLIN_yCln2_LP_2 | 631 | 637 | PF00134 | 0.542 |
DOC_MAPK_DCC_7 | 367 | 375 | PF00069 | 0.312 |
DOC_MAPK_DCC_7 | 454 | 463 | PF00069 | 0.217 |
DOC_MAPK_gen_1 | 263 | 273 | PF00069 | 0.342 |
DOC_MAPK_gen_1 | 292 | 300 | PF00069 | 0.217 |
DOC_MAPK_MEF2A_6 | 454 | 463 | PF00069 | 0.306 |
DOC_MAPK_MEF2A_6 | 575 | 582 | PF00069 | 0.457 |
DOC_PP1_RVXF_1 | 5 | 11 | PF00149 | 0.340 |
DOC_PP4_FxxP_1 | 245 | 248 | PF00568 | 0.342 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.266 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.516 |
DOC_USP7_UBL2_3 | 309 | 313 | PF12436 | 0.419 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.488 |
LIG_14-3-3_CanoR_1 | 152 | 158 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 31 | 36 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 426 | 434 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 516 | 522 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 7 | 15 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 81 | 86 | PF00244 | 0.459 |
LIG_Actin_WH2_2 | 266 | 283 | PF00022 | 0.342 |
LIG_AP2alpha_1 | 474 | 478 | PF02296 | 0.292 |
LIG_BRCT_BRCA1_1 | 284 | 288 | PF00533 | 0.379 |
LIG_BRCT_BRCA1_1 | 606 | 610 | PF00533 | 0.394 |
LIG_Clathr_ClatBox_1 | 270 | 274 | PF01394 | 0.342 |
LIG_deltaCOP1_diTrp_1 | 407 | 413 | PF00928 | 0.318 |
LIG_EH1_1 | 477 | 485 | PF00400 | 0.259 |
LIG_eIF4E_1 | 447 | 453 | PF01652 | 0.342 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.550 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.522 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.398 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.380 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.342 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.267 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.266 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.299 |
LIG_FHA_1 | 630 | 636 | PF00498 | 0.651 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.337 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.324 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.549 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.481 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.386 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.483 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.231 |
LIG_GBD_Chelix_1 | 533 | 541 | PF00786 | 0.553 |
LIG_LIR_Apic_2 | 83 | 89 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 239 | 250 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 255 | 264 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 274 | 284 | PF02991 | 0.200 |
LIG_LIR_Gen_1 | 285 | 296 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 346 | 355 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 360 | 370 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 49 | 60 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 61 | 70 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 653 | 658 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 204 | 208 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 274 | 280 | PF02991 | 0.193 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.223 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 346 | 351 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 360 | 365 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 443 | 447 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 607 | 612 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 61 | 67 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 613 | 619 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 653 | 658 | PF02991 | 0.545 |
LIG_MLH1_MIPbox_1 | 606 | 610 | PF16413 | 0.394 |
LIG_PDZ_Class_2 | 653 | 658 | PF00595 | 0.605 |
LIG_Pex14_2 | 10 | 14 | PF04695 | 0.365 |
LIG_Pex14_2 | 205 | 209 | PF04695 | 0.342 |
LIG_Pex14_2 | 385 | 389 | PF04695 | 0.267 |
LIG_Pex14_2 | 474 | 478 | PF04695 | 0.292 |
LIG_SH2_CRK | 318 | 322 | PF00017 | 0.402 |
LIG_SH2_CRK | 64 | 68 | PF00017 | 0.396 |
LIG_SH2_PTP2 | 2 | 5 | PF00017 | 0.401 |
LIG_SH2_PTP2 | 277 | 280 | PF00017 | 0.342 |
LIG_SH2_PTP2 | 577 | 580 | PF00017 | 0.497 |
LIG_SH2_SRC | 577 | 580 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 577 | 580 | PF00017 | 0.497 |
LIG_SH3_1 | 207 | 213 | PF00018 | 0.342 |
LIG_SH3_1 | 409 | 415 | PF00018 | 0.275 |
LIG_SH3_2 | 412 | 417 | PF14604 | 0.301 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.503 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.550 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.478 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.282 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.535 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.275 |
LIG_SH3_3 | 563 | 569 | PF00018 | 0.580 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.481 |
LIG_SUMO_SIM_anti_2 | 16 | 24 | PF11976 | 0.356 |
LIG_SUMO_SIM_anti_2 | 38 | 44 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 16 | 24 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 198 | 204 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 25 | 30 | PF11976 | 0.355 |
LIG_SUMO_SIM_par_1 | 269 | 274 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 38 | 44 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 595 | 600 | PF11976 | 0.415 |
LIG_WRC_WIRS_1 | 483 | 488 | PF05994 | 0.342 |
LIG_WRC_WIRS_1 | 619 | 624 | PF05994 | 0.584 |
LIG_WRC_WIRS_1 | 645 | 650 | PF05994 | 0.457 |
MOD_CDK_SPxK_1 | 1 | 7 | PF00069 | 0.400 |
MOD_CDK_SPxK_1 | 368 | 374 | PF00069 | 0.386 |
MOD_CDK_SPxxK_3 | 568 | 575 | PF00069 | 0.508 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.574 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.509 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.290 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.490 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.341 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.342 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.695 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.540 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.420 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.500 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.365 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.429 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.354 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.223 |
MOD_CK2_1 | 567 | 573 | PF00069 | 0.603 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.407 |
MOD_CMANNOS | 410 | 413 | PF00535 | 0.467 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.736 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.798 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.701 |
MOD_GlcNHglycan | 179 | 183 | PF01048 | 0.745 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.544 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.470 |
MOD_GlcNHglycan | 317 | 321 | PF01048 | 0.719 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.646 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.516 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.533 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.719 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.415 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.754 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.572 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.530 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.493 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.498 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.370 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.279 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.473 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.340 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.342 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.332 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.386 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.382 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.705 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.513 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.532 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.418 |
MOD_N-GLC_1 | 592 | 597 | PF02516 | 0.415 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.410 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.611 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.297 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.328 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.248 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.356 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.366 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.448 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.267 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.342 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.301 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.385 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.427 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.403 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.378 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.318 |
MOD_NEK2_2 | 495 | 500 | PF00069 | 0.306 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.546 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.593 |
MOD_PIKK_1 | 236 | 242 | PF00454 | 0.342 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.406 |
MOD_PIKK_1 | 464 | 470 | PF00454 | 0.342 |
MOD_PIKK_1 | 484 | 490 | PF00454 | 0.267 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.387 |
MOD_PIKK_1 | 620 | 626 | PF00454 | 0.624 |
MOD_PKA_1 | 31 | 37 | PF00069 | 0.412 |
MOD_PKA_1 | 403 | 409 | PF00069 | 0.274 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.540 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.540 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.384 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.351 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.371 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.556 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.217 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.352 |
MOD_Plk_1 | 495 | 501 | PF00069 | 0.342 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.421 |
MOD_Plk_1 | 592 | 598 | PF00069 | 0.415 |
MOD_Plk_2-3 | 145 | 151 | PF00069 | 0.560 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.433 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.387 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.292 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.217 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.301 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.318 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.402 |
MOD_Plk_4 | 604 | 610 | PF00069 | 0.408 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.492 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.346 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.417 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.421 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.565 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.614 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.342 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.431 |
MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.498 |
MOD_ProDKin_1 | 630 | 636 | PF00069 | 0.651 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.489 |
MOD_SUMO_rev_2 | 24 | 34 | PF00179 | 0.401 |
MOD_SUMO_rev_2 | 262 | 271 | PF00179 | 0.274 |
MOD_SUMO_rev_2 | 332 | 340 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 397 | 406 | PF00179 | 0.292 |
MOD_SUMO_rev_2 | 570 | 576 | PF00179 | 0.483 |
TRG_DiLeu_BaEn_3 | 16 | 22 | PF01217 | 0.402 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.238 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 577 | 580 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.393 |
TRG_ER_diArg_1 | 205 | 207 | PF00400 | 0.395 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NSV7 | Trypanosomatidae | 39% | 92% |
A0A3R7LZ26 | Trypanosoma rangeli | 40% | 100% |
A0A3S7WUF7 | Leishmania donovani | 93% | 100% |
A4H911 | Leishmania braziliensis | 79% | 92% |
A4HXE3 | Leishmania infantum | 93% | 100% |
E9AR38 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5B9G2 | Trypanosoma cruzi | 38% | 92% |