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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0034708 | methyltransferase complex | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0043527 | tRNA methyltransferase complex | 5 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4I8S1
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006396 | RNA processing | 6 | 10 |
GO:0006399 | tRNA metabolic process | 7 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008033 | tRNA processing | 8 | 10 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009451 | RNA modification | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0032259 | methylation | 2 | 11 |
GO:0034470 | ncRNA processing | 7 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034660 | ncRNA metabolic process | 6 | 10 |
GO:0036265 | RNA (guanine-N7)-methylation | 5 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0043414 | macromolecule methylation | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0030488 | tRNA methylation | 5 | 1 |
GO:0106004 | tRNA (guanine-N7)-methylation | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 419 | 423 | PF00656 | 0.468 |
CLV_C14_Caspase3-7 | 73 | 77 | PF00656 | 0.392 |
CLV_MEL_PAP_1 | 368 | 374 | PF00089 | 0.422 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.653 |
CLV_PCSK_FUR_1 | 532 | 536 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.712 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.662 |
CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 440 | 442 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.422 |
DOC_ANK_TNKS_1 | 344 | 351 | PF00023 | 0.484 |
DOC_CDC14_PxL_1 | 5 | 13 | PF14671 | 0.538 |
DOC_CYCLIN_RxL_1 | 229 | 241 | PF00134 | 0.532 |
DOC_CYCLIN_yCln2_LP_2 | 304 | 310 | PF00134 | 0.582 |
DOC_MAPK_gen_1 | 440 | 447 | PF00069 | 0.392 |
DOC_PP1_RVXF_1 | 177 | 183 | PF00149 | 0.506 |
DOC_PP1_RVXF_1 | 55 | 62 | PF00149 | 0.428 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.482 |
DOC_PP2B_LxvP_1 | 304 | 307 | PF13499 | 0.610 |
DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.451 |
DOC_PP4_FxxP_1 | 372 | 375 | PF00568 | 0.515 |
DOC_PP4_FxxP_1 | 396 | 399 | PF00568 | 0.464 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.560 |
DOC_USP7_UBL2_3 | 564 | 568 | PF12436 | 0.782 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.661 |
LIG_14-3-3_CanoR_1 | 154 | 159 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 177 | 183 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 264 | 268 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 418 | 422 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 424 | 430 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 511 | 518 | PF00244 | 0.546 |
LIG_AP2alpha_1 | 168 | 172 | PF02296 | 0.364 |
LIG_BIR_III_2 | 422 | 426 | PF00653 | 0.564 |
LIG_BRCT_BRCA1_1 | 392 | 396 | PF00533 | 0.507 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.762 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.452 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.529 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.311 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.405 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.477 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.525 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.468 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.480 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.453 |
LIG_FHA_2 | 505 | 511 | PF00498 | 0.690 |
LIG_LIR_Apic_2 | 140 | 144 | PF02991 | 0.575 |
LIG_LIR_Apic_2 | 370 | 375 | PF02991 | 0.508 |
LIG_LIR_Apic_2 | 393 | 399 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 336 | 346 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 446 | 455 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 523 | 531 | PF02991 | 0.669 |
LIG_LIR_Gen_1 | 76 | 85 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 170 | 175 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 354 | 359 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 446 | 450 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 523 | 529 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.487 |
LIG_MYND_3 | 482 | 486 | PF01753 | 0.533 |
LIG_Pex14_1 | 142 | 146 | PF04695 | 0.582 |
LIG_Pex14_2 | 168 | 172 | PF04695 | 0.364 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.559 |
LIG_SH2_GRB2like | 401 | 404 | PF00017 | 0.470 |
LIG_SH2_NCK_1 | 401 | 405 | PF00017 | 0.491 |
LIG_SH2_NCK_1 | 526 | 530 | PF00017 | 0.546 |
LIG_SH2_SRC | 146 | 149 | PF00017 | 0.574 |
LIG_SH2_SRC | 401 | 404 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 286 | 290 | PF00017 | 0.628 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.495 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.516 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.484 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.558 |
LIG_SH3_3 | 525 | 531 | PF00018 | 0.611 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.529 |
LIG_SH3_4 | 143 | 150 | PF00018 | 0.555 |
LIG_SUMO_SIM_par_1 | 185 | 191 | PF11976 | 0.567 |
LIG_TRAF2_1 | 225 | 228 | PF00917 | 0.665 |
LIG_TRAF2_1 | 498 | 501 | PF00917 | 0.743 |
LIG_WRC_WIRS_1 | 341 | 346 | PF05994 | 0.530 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.523 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.393 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.406 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.525 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.706 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.733 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.523 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.466 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.524 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.572 |
MOD_Cter_Amidation | 566 | 569 | PF01082 | 0.703 |
MOD_GlcNHglycan | 227 | 232 | PF01048 | 0.562 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.523 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.560 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.750 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.635 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.393 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.440 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.495 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.273 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.377 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.337 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.621 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.437 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.505 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.542 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.618 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.465 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.596 |
MOD_LATS_1 | 151 | 157 | PF00433 | 0.424 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.654 |
MOD_N-GLC_1 | 300 | 305 | PF02516 | 0.668 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.546 |
MOD_N-GLC_1 | 547 | 552 | PF02516 | 0.742 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.536 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.646 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.400 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.550 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.484 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.561 |
MOD_NEK2_2 | 405 | 410 | PF00069 | 0.404 |
MOD_OFUCOSY | 234 | 240 | PF10250 | 0.427 |
MOD_PKA_1 | 120 | 126 | PF00069 | 0.719 |
MOD_PKA_1 | 153 | 159 | PF00069 | 0.411 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.719 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.411 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.488 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.381 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.439 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.508 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.575 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.536 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.644 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.668 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.504 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.456 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.534 |
MOD_Plk_2-3 | 510 | 516 | PF00069 | 0.652 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.356 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.435 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.483 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.474 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.432 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.547 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.470 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.512 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.654 |
MOD_SUMO_for_1 | 137 | 140 | PF00179 | 0.598 |
MOD_SUMO_rev_2 | 73 | 80 | PF00179 | 0.430 |
TRG_DiLeu_BaEn_1 | 336 | 341 | PF01217 | 0.452 |
TRG_DiLeu_BaEn_2 | 432 | 438 | PF01217 | 0.534 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 526 | 529 | PF00928 | 0.545 |
TRG_ER_diArg_1 | 176 | 179 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 235 | 237 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 344 | 347 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 531 | 534 | PF00400 | 0.589 |
TRG_NES_CRM1_1 | 54 | 66 | PF08389 | 0.546 |
TRG_NLS_MonoExtC_3 | 567 | 573 | PF00514 | 0.724 |
TRG_NLS_MonoExtN_4 | 120 | 125 | PF00514 | 0.670 |
TRG_Pf-PMV_PEXEL_1 | 3 | 7 | PF00026 | 0.658 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL73 | Leptomonas seymouri | 67% | 100% |
A0A1X0P0S8 | Trypanosomatidae | 29% | 100% |
A0A3Q8IGQ7 | Leishmania donovani | 99% | 100% |
A0A422N539 | Trypanosoma rangeli | 32% | 100% |
A4HL95 | Leishmania braziliensis | 79% | 99% |
D0A4R4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9B3N7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q4F0 | Leishmania major | 94% | 100% |
V5D2Q1 | Trypanosoma cruzi | 32% | 100% |