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: E9B3N7
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 | 420 | 424 | PF00656 | 0.473 |
CLV_MEL_PAP_1 | 369 | 375 | PF00089 | 0.440 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.662 |
CLV_PCSK_FUR_1 | 533 | 537 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 569 | 571 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 441 | 443 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 569 | 571 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.435 |
DOC_CDC14_PxL_1 | 5 | 13 | PF14671 | 0.531 |
DOC_CYCLIN_RxL_1 | 230 | 242 | PF00134 | 0.533 |
DOC_CYCLIN_yCln2_LP_2 | 305 | 311 | PF00134 | 0.613 |
DOC_MAPK_gen_1 | 441 | 448 | PF00069 | 0.395 |
DOC_PP1_RVXF_1 | 178 | 184 | PF00149 | 0.503 |
DOC_PP1_RVXF_1 | 55 | 62 | PF00149 | 0.425 |
DOC_PP2B_LxvP_1 | 214 | 217 | PF13499 | 0.484 |
DOC_PP2B_LxvP_1 | 305 | 308 | PF13499 | 0.659 |
DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.448 |
DOC_PP4_FxxP_1 | 373 | 376 | PF00568 | 0.535 |
DOC_PP4_FxxP_1 | 397 | 400 | PF00568 | 0.471 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.566 |
DOC_USP7_UBL2_3 | 565 | 569 | PF12436 | 0.809 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.666 |
LIG_14-3-3_CanoR_1 | 155 | 160 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 265 | 269 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 419 | 423 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 512 | 519 | PF00244 | 0.532 |
LIG_AP2alpha_1 | 169 | 173 | PF02296 | 0.358 |
LIG_BIR_III_2 | 423 | 427 | PF00653 | 0.573 |
LIG_BRCT_BRCA1_1 | 393 | 397 | PF00533 | 0.507 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.778 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.448 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.530 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.303 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.405 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.491 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.543 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.477 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.533 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.489 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.477 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.460 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.681 |
LIG_LIR_Apic_2 | 141 | 145 | PF02991 | 0.586 |
LIG_LIR_Apic_2 | 371 | 376 | PF02991 | 0.527 |
LIG_LIR_Apic_2 | 394 | 400 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 337 | 347 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 447 | 456 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 524 | 532 | PF02991 | 0.673 |
LIG_LIR_Gen_1 | 76 | 85 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 337 | 342 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 447 | 451 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 524 | 530 | PF02991 | 0.663 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.486 |
LIG_MYND_3 | 483 | 487 | PF01753 | 0.536 |
LIG_Pex14_1 | 143 | 147 | PF04695 | 0.586 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.358 |
LIG_SH2_CRK | 402 | 406 | PF00017 | 0.589 |
LIG_SH2_GRB2like | 402 | 405 | PF00017 | 0.496 |
LIG_SH2_NCK_1 | 402 | 406 | PF00017 | 0.522 |
LIG_SH2_NCK_1 | 527 | 531 | PF00017 | 0.550 |
LIG_SH2_SRC | 147 | 150 | PF00017 | 0.572 |
LIG_SH2_SRC | 402 | 405 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 287 | 291 | PF00017 | 0.626 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.345 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.527 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.403 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.498 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.563 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.613 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.528 |
LIG_SH3_4 | 144 | 151 | PF00018 | 0.554 |
LIG_SUMO_SIM_par_1 | 186 | 192 | PF11976 | 0.567 |
LIG_TRAF2_1 | 226 | 229 | PF00917 | 0.653 |
LIG_TRAF2_1 | 499 | 502 | PF00917 | 0.730 |
LIG_WRC_WIRS_1 | 342 | 347 | PF05994 | 0.546 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.395 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.520 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.395 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.416 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.325 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.532 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.747 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.520 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.470 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.532 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.557 |
MOD_Cter_Amidation | 567 | 570 | PF01082 | 0.731 |
MOD_DYRK1A_RPxSP_1 | 346 | 350 | PF00069 | 0.317 |
MOD_GlcNHglycan | 228 | 233 | PF01048 | 0.557 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.525 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.588 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.790 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.653 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.389 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.437 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.494 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.273 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.377 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.330 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.611 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.450 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.514 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.547 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.622 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.485 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.347 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.644 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.657 |
MOD_LATS_1 | 152 | 158 | PF00433 | 0.420 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.643 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.705 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.527 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.561 |
MOD_N-GLC_1 | 548 | 553 | PF02516 | 0.783 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.534 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.652 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.403 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.558 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.501 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.567 |
MOD_NEK2_2 | 406 | 411 | PF00069 | 0.434 |
MOD_OFUCOSY | 235 | 241 | PF10250 | 0.430 |
MOD_PKA_1 | 120 | 126 | PF00069 | 0.723 |
MOD_PKA_1 | 154 | 160 | PF00069 | 0.407 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.723 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.407 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.485 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.383 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.453 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.515 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.560 |
MOD_PKB_1 | 570 | 578 | PF00069 | 0.600 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.540 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.643 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.706 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.441 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.519 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.465 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.533 |
MOD_Plk_2-3 | 511 | 517 | PF00069 | 0.638 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.352 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.428 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.344 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.497 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.489 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.437 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.553 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.473 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.511 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.404 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.658 |
MOD_SUMO_for_1 | 138 | 141 | PF00179 | 0.629 |
MOD_SUMO_rev_2 | 73 | 80 | PF00179 | 0.428 |
TRG_DiLeu_BaEn_1 | 337 | 342 | PF01217 | 0.469 |
TRG_DiLeu_BaEn_2 | 433 | 439 | PF01217 | 0.544 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 527 | 530 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 177 | 180 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 236 | 238 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 345 | 348 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 532 | 535 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 570 | 573 | PF00400 | 0.607 |
TRG_NES_CRM1_1 | 54 | 66 | PF08389 | 0.543 |
TRG_NLS_MonoExtC_3 | 568 | 574 | PF00514 | 0.749 |
TRG_NLS_MonoExtN_4 | 120 | 125 | PF00514 | 0.675 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL73 | Leptomonas seymouri | 66% | 100% |
A0A1X0P0S8 | Trypanosomatidae | 30% | 100% |
A0A3Q8IGQ7 | Leishmania donovani | 93% | 100% |
A0A422N539 | Trypanosoma rangeli | 33% | 100% |
A4HL95 | Leishmania braziliensis | 79% | 99% |
A4I8S1 | Leishmania infantum | 94% | 100% |
D0A4R4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
Q4Q4F0 | Leishmania major | 93% | 100% |
V5D2Q1 | Trypanosoma cruzi | 32% | 100% |