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 | 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: A4HL95
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: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: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:1901360 | organic cyclic compound metabolic process | 3 | 12 |
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 | 113 | 117 | PF00656 | 0.747 |
CLV_C14_Caspase3-7 | 368 | 372 | PF00656 | 0.592 |
CLV_C14_Caspase3-7 | 536 | 540 | PF00656 | 0.719 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 559 | 561 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.564 |
CLV_PCSK_FUR_1 | 529 | 533 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.754 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.678 |
CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 299 | 301 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 438 | 440 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.435 |
DEG_SPOP_SBC_1 | 365 | 369 | PF00917 | 0.387 |
DOC_CYCLIN_RxL_1 | 230 | 242 | PF00134 | 0.507 |
DOC_CYCLIN_yCln2_LP_2 | 305 | 311 | PF00134 | 0.599 |
DOC_MAPK_gen_1 | 18 | 25 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 438 | 448 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 442 | 450 | PF00069 | 0.278 |
DOC_PP1_RVXF_1 | 178 | 184 | PF00149 | 0.505 |
DOC_PP1_RVXF_1 | 440 | 446 | PF00149 | 0.267 |
DOC_PP1_RVXF_1 | 55 | 62 | PF00149 | 0.440 |
DOC_PP2B_LxvP_1 | 214 | 217 | PF13499 | 0.477 |
DOC_PP2B_LxvP_1 | 305 | 308 | PF13499 | 0.644 |
DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.465 |
DOC_PP4_FxxP_1 | 373 | 376 | PF00568 | 0.564 |
DOC_PP4_FxxP_1 | 394 | 397 | PF00568 | 0.432 |
DOC_PP4_FxxP_1 | 556 | 559 | PF00568 | 0.541 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.599 |
DOC_USP7_MATH_2 | 331 | 337 | PF00917 | 0.360 |
DOC_USP7_UBL2_3 | 299 | 303 | PF12436 | 0.477 |
DOC_USP7_UBL2_3 | 561 | 565 | PF12436 | 0.784 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.542 |
LIG_14-3-3_CanoR_1 | 120 | 129 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 155 | 160 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 300 | 306 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 389 | 397 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 442 | 446 | PF00244 | 0.263 |
LIG_BIR_III_2 | 420 | 424 | PF00653 | 0.575 |
LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.424 |
LIG_BRCT_BRCA1_1 | 390 | 394 | PF00533 | 0.508 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.790 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.433 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.544 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.387 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.329 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.444 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.549 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.420 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.491 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.549 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.486 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.465 |
LIG_Integrin_isoDGR_2 | 440 | 442 | PF01839 | 0.422 |
LIG_LIR_Apic_2 | 141 | 145 | PF02991 | 0.580 |
LIG_LIR_Apic_2 | 371 | 376 | PF02991 | 0.581 |
LIG_LIR_Apic_2 | 391 | 397 | PF02991 | 0.445 |
LIG_LIR_Apic_2 | 554 | 559 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 336 | 347 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 444 | 452 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 520 | 528 | PF02991 | 0.680 |
LIG_LIR_Gen_1 | 76 | 85 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 336 | 342 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 444 | 448 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 520 | 526 | PF02991 | 0.673 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.500 |
LIG_MYND_3 | 479 | 483 | PF01753 | 0.534 |
LIG_PDZ_Class_2 | 567 | 572 | PF00595 | 0.528 |
LIG_Pex14_1 | 143 | 147 | PF04695 | 0.578 |
LIG_Pex14_2 | 395 | 399 | PF04695 | 0.255 |
LIG_Rb_LxCxE_1 | 273 | 296 | PF01857 | 0.386 |
LIG_SH2_NCK_1 | 523 | 527 | PF00017 | 0.570 |
LIG_SH2_SRC | 147 | 150 | PF00017 | 0.561 |
LIG_SH2_STAP1 | 169 | 173 | PF00017 | 0.267 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.508 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.469 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.479 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.539 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.505 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.540 |
LIG_SH3_4 | 144 | 151 | PF00018 | 0.551 |
LIG_SUMO_SIM_par_1 | 186 | 192 | PF11976 | 0.567 |
LIG_SUMO_SIM_par_1 | 468 | 474 | PF11976 | 0.544 |
LIG_TRAF2_1 | 226 | 229 | PF00917 | 0.686 |
LIG_TRAF2_1 | 494 | 497 | PF00917 | 0.741 |
LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.544 |
LIG_WRC_WIRS_1 | 342 | 347 | PF05994 | 0.536 |
MOD_CDC14_SPxK_1 | 558 | 561 | PF00782 | 0.537 |
MOD_CDK_SPK_2 | 555 | 560 | PF00069 | 0.542 |
MOD_CDK_SPxK_1 | 555 | 561 | PF00069 | 0.541 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.784 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.524 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.381 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.378 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.485 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.564 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.420 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.524 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.516 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.503 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.573 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.725 |
MOD_GlcNHglycan | 228 | 233 | PF01048 | 0.561 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.578 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.607 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.586 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.403 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.437 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.459 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.391 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.612 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.392 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.551 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.499 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.523 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.624 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.456 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.395 |
MOD_LATS_1 | 152 | 158 | PF00433 | 0.405 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.705 |
MOD_N-GLC_1 | 429 | 434 | PF02516 | 0.413 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.547 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.649 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.564 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.402 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.540 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.619 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.495 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.578 |
MOD_OFUCOSY | 235 | 241 | PF10250 | 0.418 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.461 |
MOD_PKA_1 | 120 | 126 | PF00069 | 0.744 |
MOD_PKA_1 | 154 | 160 | PF00069 | 0.396 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.744 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.412 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.492 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.361 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.505 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.266 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.705 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.473 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.480 |
MOD_Plk_2-3 | 507 | 513 | PF00069 | 0.643 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.364 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.338 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.448 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.473 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.456 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.582 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.454 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.518 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.394 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.684 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.386 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.587 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.541 |
MOD_SUMO_for_1 | 138 | 141 | PF00179 | 0.611 |
MOD_SUMO_rev_2 | 558 | 568 | PF00179 | 0.655 |
MOD_SUMO_rev_2 | 73 | 80 | PF00179 | 0.442 |
TRG_DiLeu_BaEn_1 | 337 | 342 | PF01217 | 0.469 |
TRG_DiLeu_BaEn_2 | 430 | 436 | PF01217 | 0.548 |
TRG_DiLeu_BaLyEn_6 | 25 | 30 | PF01217 | 0.272 |
TRG_ENDOCYTIC_2 | 523 | 526 | PF00928 | 0.572 |
TRG_ER_diArg_1 | 177 | 180 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 236 | 238 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 528 | 531 | PF00400 | 0.597 |
TRG_NES_CRM1_1 | 54 | 66 | PF08389 | 0.547 |
TRG_NLS_MonoExtC_3 | 565 | 571 | PF00514 | 0.603 |
TRG_NLS_MonoExtN_4 | 565 | 570 | PF00514 | 0.743 |
TRG_Pf-PMV_PEXEL_1 | 3 | 7 | PF00026 | 0.661 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL73 | Leptomonas seymouri | 65% | 100% |
A0A0S4IWR1 | Bodo saltans | 22% | 100% |
A0A1X0P0S8 | Trypanosomatidae | 30% | 100% |
A0A3Q8IGQ7 | Leishmania donovani | 79% | 99% |
A0A422N539 | Trypanosoma rangeli | 32% | 100% |
A4I8S1 | Leishmania infantum | 79% | 99% |
D0A4R4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B3N7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 99% |
Q4Q4F0 | Leishmania major | 79% | 100% |
V5D2Q1 | Trypanosoma cruzi | 32% | 100% |