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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005829 | cytosol | 2 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0034708 | methyltransferase complex | 4 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0043527 | tRNA methyltransferase complex | 5 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
Related structures:
AlphaFold database: Q4Q4F0
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006399 | tRNA metabolic process | 7 | 11 |
GO:0006400 | tRNA modification | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008033 | tRNA processing | 8 | 11 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0030488 | tRNA methylation | 5 | 2 |
GO:0032259 | methylation | 2 | 12 |
GO:0034470 | ncRNA processing | 7 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 11 |
GO:0036265 | RNA (guanine-N7)-methylation | 5 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043414 | macromolecule methylation | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:0106004 | tRNA (guanine-N7)-methylation | 6 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 370 | 374 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 422 | 426 | PF00656 | 0.418 |
CLV_C14_Caspase3-7 | 542 | 546 | PF00656 | 0.652 |
CLV_C14_Caspase3-7 | 73 | 77 | PF00656 | 0.349 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.628 |
CLV_PCSK_FUR_1 | 535 | 539 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.622 |
CLV_PCSK_PC1ET2_1 | 156 | 158 | PF00082 | 0.374 |
CLV_PCSK_PC1ET2_1 | 443 | 445 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.388 |
DOC_ANK_TNKS_1 | 347 | 354 | PF00023 | 0.410 |
DOC_CDC14_PxL_1 | 5 | 13 | PF14671 | 0.442 |
DOC_CYCLIN_RxL_1 | 199 | 209 | PF00134 | 0.287 |
DOC_CYCLIN_RxL_1 | 232 | 244 | PF00134 | 0.501 |
DOC_CYCLIN_yCln2_LP_2 | 307 | 313 | PF00134 | 0.466 |
DOC_MAPK_gen_1 | 443 | 450 | PF00069 | 0.349 |
DOC_PP1_RVXF_1 | 180 | 186 | PF00149 | 0.480 |
DOC_PP1_RVXF_1 | 55 | 62 | PF00149 | 0.382 |
DOC_PP2B_LxvP_1 | 216 | 219 | PF13499 | 0.442 |
DOC_PP2B_LxvP_1 | 307 | 310 | PF13499 | 0.506 |
DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.406 |
DOC_PP4_FxxP_1 | 399 | 402 | PF00568 | 0.387 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.553 |
DOC_USP7_UBL2_3 | 567 | 571 | PF12436 | 0.673 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.501 |
LIG_14-3-3_CanoR_1 | 157 | 162 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 180 | 186 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 267 | 271 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 421 | 425 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 514 | 521 | PF00244 | 0.441 |
LIG_AP2alpha_1 | 171 | 175 | PF02296 | 0.312 |
LIG_APCC_ABBA_1 | 168 | 173 | PF00400 | 0.229 |
LIG_BIR_III_2 | 425 | 429 | PF00653 | 0.430 |
LIG_BRCT_BRCA1_1 | 395 | 399 | PF00533 | 0.375 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.641 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.388 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.507 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.334 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.410 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.538 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.429 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.439 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.404 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.647 |
LIG_LIR_Apic_2 | 143 | 147 | PF02991 | 0.560 |
LIG_LIR_Apic_2 | 396 | 402 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 339 | 349 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 449 | 458 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 526 | 534 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 339 | 344 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 373 | 378 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 449 | 453 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.521 |
LIG_MYND_3 | 485 | 489 | PF01753 | 0.514 |
LIG_Pex14_1 | 145 | 149 | PF04695 | 0.459 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.312 |
LIG_SH2_CRK | 404 | 408 | PF00017 | 0.573 |
LIG_SH2_GRB2like | 404 | 407 | PF00017 | 0.461 |
LIG_SH2_NCK_1 | 404 | 408 | PF00017 | 0.404 |
LIG_SH2_NCK_1 | 529 | 533 | PF00017 | 0.494 |
LIG_SH2_SRC | 149 | 152 | PF00017 | 0.441 |
LIG_SH2_SRC | 404 | 407 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 311 | 315 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.497 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.553 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.539 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.503 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.500 |
LIG_SH3_4 | 146 | 153 | PF00018 | 0.526 |
LIG_SUMO_SIM_par_1 | 188 | 194 | PF11976 | 0.542 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.578 |
LIG_TRAF2_1 | 501 | 504 | PF00917 | 0.611 |
LIG_WRC_WIRS_1 | 344 | 349 | PF05994 | 0.509 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.741 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.357 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.492 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.325 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.364 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.477 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.701 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.733 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.492 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.517 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.483 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.557 |
MOD_CK2_1 | 505 | 511 | PF00069 | 0.644 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.524 |
MOD_Cter_Amidation | 569 | 572 | PF01082 | 0.621 |
MOD_GlcNHglycan | 230 | 235 | PF01048 | 0.553 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.386 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.578 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.759 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.607 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.351 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.391 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.432 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.341 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.363 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.544 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.394 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.484 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.490 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.587 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.430 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.599 |
MOD_LATS_1 | 154 | 160 | PF00433 | 0.358 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.627 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.564 |
MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.560 |
MOD_N-GLC_1 | 550 | 555 | PF02516 | 0.748 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.483 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.588 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.361 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.546 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.457 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.529 |
MOD_PKA_1 | 122 | 128 | PF00069 | 0.701 |
MOD_PKA_1 | 156 | 162 | PF00069 | 0.349 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.701 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.364 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.451 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.320 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.384 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.465 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.626 |
MOD_PKB_1 | 237 | 245 | PF00069 | 0.382 |
MOD_PKB_1 | 537 | 545 | PF00069 | 0.572 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.524 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.620 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.690 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.471 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.405 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.511 |
MOD_Plk_2-3 | 107 | 113 | PF00069 | 0.686 |
MOD_Plk_2-3 | 513 | 519 | PF00069 | 0.516 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.422 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.425 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.385 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.534 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.404 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.473 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.658 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.511 |
MOD_SUMO_for_1 | 140 | 143 | PF00179 | 0.596 |
MOD_SUMO_rev_2 | 73 | 80 | PF00179 | 0.388 |
TRG_DiLeu_BaEn_1 | 339 | 344 | PF01217 | 0.424 |
TRG_DiLeu_BaEn_2 | 435 | 441 | PF01217 | 0.404 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.492 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 237 | 239 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 534 | 537 | PF00400 | 0.536 |
TRG_NES_CRM1_1 | 54 | 66 | PF08389 | 0.415 |
TRG_NLS_MonoExtC_3 | 570 | 575 | PF00514 | 0.671 |
TRG_NLS_MonoExtN_4 | 122 | 127 | PF00514 | 0.584 |
TRG_NLS_MonoExtN_4 | 571 | 576 | PF00514 | 0.714 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.285 |
TRG_Pf-PMV_PEXEL_1 | 3 | 7 | PF00026 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL73 | Leptomonas seymouri | 65% | 100% |
A0A0S4IWR1 | Bodo saltans | 23% | 100% |
A0A1X0P0S8 | Trypanosomatidae | 30% | 100% |
A0A3Q8IGQ7 | Leishmania donovani | 94% | 100% |
A0A422N539 | Trypanosoma rangeli | 32% | 100% |
A4HL95 | Leishmania braziliensis | 79% | 100% |
A4I8S1 | Leishmania infantum | 94% | 100% |
D0A4R4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9B3N7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5D2Q1 | Trypanosoma cruzi | 33% | 100% |