Uncharacterized Protein, Uncharacterized
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: A0A3Q8IF44
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0008643 | carbohydrate transport | 5 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.542 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 259 | 261 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.383 |
DEG_APCC_DBOX_1 | 63 | 71 | PF00400 | 0.292 |
DOC_CDC14_PxL_1 | 498 | 506 | PF14671 | 0.354 |
DOC_MAPK_gen_1 | 126 | 135 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 126 | 135 | PF00069 | 0.557 |
DOC_MAPK_MEF2A_6 | 408 | 417 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 427 | 436 | PF00069 | 0.342 |
DOC_PP2B_PxIxI_1 | 130 | 136 | PF00149 | 0.496 |
DOC_PP4_FxxP_1 | 313 | 316 | PF00568 | 0.354 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.371 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.415 |
LIG_14-3-3_CanoR_1 | 272 | 276 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 281 | 285 | PF00244 | 0.552 |
LIG_Actin_WH2_2 | 413 | 429 | PF00022 | 0.304 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.685 |
LIG_deltaCOP1_diTrp_1 | 36 | 44 | PF00928 | 0.590 |
LIG_EH_1 | 377 | 381 | PF12763 | 0.488 |
LIG_eIF4E_1 | 236 | 242 | PF01652 | 0.259 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.667 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.469 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.394 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.392 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.434 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.324 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.606 |
LIG_LIR_Gen_1 | 103 | 114 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 154 | 164 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 171 | 181 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 309 | 318 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 394 | 398 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.527 |
LIG_NRBOX | 347 | 353 | PF00104 | 0.348 |
LIG_Pex14_1 | 39 | 43 | PF04695 | 0.626 |
LIG_Pex14_2 | 298 | 302 | PF04695 | 0.384 |
LIG_Pex14_2 | 304 | 308 | PF04695 | 0.322 |
LIG_Pex14_2 | 392 | 396 | PF04695 | 0.302 |
LIG_PTB_Apo_2 | 318 | 325 | PF02174 | 0.400 |
LIG_SH2_CRK | 106 | 110 | PF00017 | 0.377 |
LIG_SH2_GRB2like | 233 | 236 | PF00017 | 0.306 |
LIG_SH2_NCK_1 | 445 | 449 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.372 |
LIG_SH2_STAP1 | 157 | 161 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 330 | 334 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 357 | 361 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 445 | 449 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 453 | 457 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 536 | 540 | PF00017 | 0.656 |
LIG_SH2_STAT3 | 362 | 365 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.383 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.380 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.364 |
LIG_TYR_ITIM | 104 | 109 | PF00017 | 0.353 |
LIG_UBA3_1 | 251 | 259 | PF00899 | 0.299 |
LIG_Vh1_VBS_1 | 189 | 207 | PF01044 | 0.525 |
LIG_WRC_WIRS_1 | 392 | 397 | PF05994 | 0.390 |
LIG_WRC_WIRS_1 | 82 | 87 | PF05994 | 0.366 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.714 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.579 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.703 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.429 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.413 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.372 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.603 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.612 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.685 |
MOD_GlcNHglycan | 195 | 199 | PF01048 | 0.376 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.362 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.447 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.392 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.603 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.462 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.392 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.323 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.634 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.328 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.508 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.323 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.306 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.658 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.343 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.350 |
MOD_LATS_1 | 23 | 29 | PF00433 | 0.669 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.670 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.437 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.447 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.380 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.345 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.474 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.571 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.347 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.670 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.308 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.387 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.398 |
MOD_NEK2_2 | 391 | 396 | PF00069 | 0.334 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.499 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.699 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.338 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.651 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.702 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.662 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.551 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.685 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.602 |
MOD_Plk_1 | 509 | 515 | PF00069 | 0.683 |
MOD_Plk_1 | 519 | 525 | PF00069 | 0.702 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.502 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.381 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.292 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.431 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.301 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.644 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.501 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.302 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.349 |
TRG_ER_diArg_1 | 266 | 268 | PF00400 | 0.666 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYC7 | Leptomonas seymouri | 54% | 99% |
A0A0N1I3H1 | Leptomonas seymouri | 29% | 80% |
A0A3Q8ILR5 | Leishmania donovani | 26% | 100% |
A4HIW8 | Leishmania braziliensis | 81% | 100% |
A4HL09 | Leishmania braziliensis | 27% | 98% |
A4I8J0 | Leishmania infantum | 26% | 99% |
E9AHK6 | Leishmania infantum | 100% | 100% |
E9B1F2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9B3F0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 97% |
Q4Q4Q0 | Leishmania major | 25% | 100% |
Q4Q6R0 | Leishmania major | 93% | 100% |