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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3Q8IHB0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 4 |
GO:0008104 | protein localization | 4 | 4 |
GO:0009966 | regulation of signal transduction | 4 | 4 |
GO:0009967 | positive regulation of signal transduction | 5 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0010646 | regulation of cell communication | 4 | 4 |
GO:0010647 | positive regulation of cell communication | 5 | 4 |
GO:0015031 | protein transport | 4 | 4 |
GO:0023051 | regulation of signaling | 3 | 4 |
GO:0023056 | positive regulation of signaling | 4 | 4 |
GO:0032006 | regulation of TOR signaling | 6 | 4 |
GO:0032008 | positive regulation of TOR signaling | 7 | 4 |
GO:0033036 | macromolecule localization | 2 | 4 |
GO:0045184 | establishment of protein localization | 3 | 4 |
GO:0048518 | positive regulation of biological process | 3 | 4 |
GO:0048522 | positive regulation of cellular process | 4 | 4 |
GO:0048583 | regulation of response to stimulus | 3 | 4 |
GO:0048584 | positive regulation of response to stimulus | 4 | 4 |
GO:0050789 | regulation of biological process | 2 | 4 |
GO:0050794 | regulation of cellular process | 3 | 4 |
GO:0051179 | localization | 1 | 4 |
GO:0051234 | establishment of localization | 2 | 4 |
GO:0051641 | cellular localization | 2 | 4 |
GO:0065007 | biological regulation | 1 | 4 |
GO:0070727 | cellular macromolecule localization | 3 | 4 |
GO:0071702 | organic substance transport | 4 | 4 |
GO:0071705 | nitrogen compound transport | 4 | 4 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 4 |
GO:1902533 | positive regulation of intracellular signal transduction | 6 | 4 |
GO:1903432 | regulation of TORC1 signaling | 7 | 4 |
GO:1904263 | positive regulation of TORC1 signaling | 8 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.806 |
CLV_C14_Caspase3-7 | 25 | 29 | PF00656 | 0.760 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.489 |
CLV_PCSK_FUR_1 | 302 | 306 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.565 |
CLV_PCSK_PC1ET2_1 | 514 | 516 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.431 |
DEG_SPOP_SBC_1 | 13 | 17 | PF00917 | 0.702 |
DEG_SPOP_SBC_1 | 293 | 297 | PF00917 | 0.587 |
DOC_CKS1_1 | 132 | 137 | PF01111 | 0.593 |
DOC_CKS1_1 | 68 | 73 | PF01111 | 0.599 |
DOC_CYCLIN_RxL_1 | 265 | 276 | PF00134 | 0.520 |
DOC_MAPK_gen_1 | 219 | 227 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 302 | 311 | PF00069 | 0.593 |
DOC_MAPK_gen_1 | 514 | 522 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 219 | 227 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 368 | 375 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 514 | 522 | PF00069 | 0.559 |
DOC_MAPK_NFAT4_5 | 368 | 376 | PF00069 | 0.389 |
DOC_PP1_RVXF_1 | 137 | 144 | PF00149 | 0.624 |
DOC_PP1_RVXF_1 | 356 | 363 | PF00149 | 0.393 |
DOC_PP1_RVXF_1 | 380 | 387 | PF00149 | 0.462 |
DOC_PP1_RVXF_1 | 440 | 446 | PF00149 | 0.537 |
DOC_PP2B_LxvP_1 | 120 | 123 | PF13499 | 0.619 |
DOC_PP2B_LxvP_1 | 270 | 273 | PF13499 | 0.515 |
DOC_PP4_FxxP_1 | 386 | 389 | PF00568 | 0.439 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.595 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.554 |
LIG_14-3-3_CanoR_1 | 186 | 194 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 21 | 30 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 228 | 237 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 268 | 273 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 523 | 531 | PF00244 | 0.526 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.419 |
LIG_CSL_BTD_1 | 361 | 364 | PF09270 | 0.454 |
LIG_deltaCOP1_diTrp_1 | 161 | 167 | PF00928 | 0.461 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.435 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.540 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.513 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.473 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.490 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.524 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.430 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.464 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.594 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.662 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.490 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.577 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.524 |
LIG_LIR_Apic_2 | 467 | 473 | PF02991 | 0.568 |
LIG_LIR_Apic_2 | 67 | 71 | PF02991 | 0.625 |
LIG_LIR_Gen_1 | 106 | 114 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 343 | 353 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 369 | 377 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 106 | 110 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 369 | 373 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 40 | 44 | PF02991 | 0.572 |
LIG_Pex14_1 | 41 | 45 | PF04695 | 0.607 |
LIG_Pex14_1 | 464 | 468 | PF04695 | 0.549 |
LIG_SH2_CRK | 346 | 350 | PF00017 | 0.574 |
LIG_SH2_CRK | 531 | 535 | PF00017 | 0.733 |
LIG_SH2_CRK | 68 | 72 | PF00017 | 0.643 |
LIG_SH2_SRC | 470 | 473 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 32 | 36 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.510 |
LIG_TRAF2_1 | 426 | 429 | PF00917 | 0.501 |
LIG_TRAF2_1 | 436 | 439 | PF00917 | 0.463 |
LIG_TYR_ITIM | 344 | 349 | PF00017 | 0.492 |
LIG_UBA3_1 | 93 | 100 | PF00899 | 0.468 |
MOD_CDC14_SPxK_1 | 355 | 358 | PF00782 | 0.342 |
MOD_CDK_SPxK_1 | 352 | 358 | PF00069 | 0.377 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.517 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.486 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.420 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.504 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.678 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.558 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.504 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.556 |
MOD_CMANNOS | 164 | 167 | PF00535 | 0.392 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.751 |
MOD_GlcNHglycan | 288 | 292 | PF01048 | 0.768 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.706 |
MOD_GlcNHglycan | 314 | 318 | PF01048 | 0.327 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.555 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.451 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.564 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.642 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.535 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.665 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.439 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.362 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.587 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.686 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.458 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.511 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.362 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.474 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.471 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.537 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.508 |
MOD_LATS_1 | 303 | 309 | PF00433 | 0.379 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.524 |
MOD_N-GLC_1 | 445 | 450 | PF02516 | 0.484 |
MOD_N-GLC_1 | 479 | 484 | PF02516 | 0.700 |
MOD_N-GLC_1 | 52 | 57 | PF02516 | 0.643 |
MOD_N-GLC_2 | 89 | 91 | PF02516 | 0.560 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.490 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.700 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.526 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.623 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.494 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.754 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.555 |
MOD_PKA_1 | 305 | 311 | PF00069 | 0.324 |
MOD_PKA_1 | 523 | 529 | PF00069 | 0.510 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.426 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.525 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.691 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.634 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.512 |
MOD_PKA_2 | 522 | 528 | PF00069 | 0.619 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.467 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.520 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.601 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.491 |
MOD_Plk_1 | 503 | 509 | PF00069 | 0.661 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.584 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.727 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.449 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.570 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.459 |
MOD_Plk_4 | 503 | 509 | PF00069 | 0.592 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.610 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.438 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.700 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.747 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.509 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.419 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.530 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.557 |
TRG_DiLeu_BaEn_1 | 315 | 320 | PF01217 | 0.424 |
TRG_DiLeu_BaEn_4 | 438 | 444 | PF01217 | 0.441 |
TRG_DiLeu_BaLyEn_6 | 136 | 141 | PF01217 | 0.649 |
TRG_DiLeu_BaLyEn_6 | 89 | 94 | PF01217 | 0.499 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 531 | 534 | PF00928 | 0.745 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 302 | 305 | PF00400 | 0.673 |
TRG_ER_diArg_1 | 386 | 388 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 522 | 524 | PF00400 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 139 | 144 | PF00026 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3R7 | Leptomonas seymouri | 61% | 90% |
A0A1X0P9T6 | Trypanosomatidae | 34% | 100% |
A0A3R7N181 | Trypanosoma rangeli | 33% | 100% |
A4HAW4 | Leishmania braziliensis | 79% | 100% |
A4IA24 | Leishmania infantum | 100% | 100% |
C9ZMJ8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9B539 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q2U7 | Leishmania major | 93% | 100% |
V5BFU9 | Trypanosoma cruzi | 32% | 100% |