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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0030684 | preribosome | 3 | 1 |
GO:0032040 | small-subunit processome | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7X1D4
Term | Name | Level | Count |
---|---|---|---|
GO:0000462 | maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0030490 | maturation of SSU-rRNA | 9 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 126 | 130 | PF00656 | 0.604 |
CLV_C14_Caspase3-7 | 15 | 19 | PF00656 | 0.713 |
CLV_C14_Caspase3-7 | 27 | 31 | PF00656 | 0.706 |
CLV_C14_Caspase3-7 | 447 | 451 | PF00656 | 0.702 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 510 | 512 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.505 |
CLV_PCSK_FUR_1 | 301 | 305 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.321 |
CLV_PCSK_PC1ET2_1 | 10 | 12 | PF00082 | 0.659 |
CLV_PCSK_PC7_1 | 515 | 521 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.733 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.746 |
CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.321 |
CLV_Separin_Metazoa | 385 | 389 | PF03568 | 0.641 |
DEG_APCC_DBOX_1 | 243 | 251 | PF00400 | 0.460 |
DEG_APCC_DBOX_1 | 303 | 311 | PF00400 | 0.507 |
DOC_CYCLIN_RxL_1 | 162 | 172 | PF00134 | 0.458 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 198 | 204 | PF00134 | 0.485 |
DOC_MAPK_gen_1 | 519 | 528 | PF00069 | 0.321 |
DOC_MAPK_RevD_3 | 105 | 119 | PF00069 | 0.610 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.806 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.533 |
DOC_USP7_UBL2_3 | 405 | 409 | PF12436 | 0.752 |
DOC_USP7_UBL2_3 | 492 | 496 | PF12436 | 0.321 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.623 |
DOC_USP7_UBL2_3 | 94 | 98 | PF12436 | 0.566 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.507 |
LIG_14-3-3_CanoR_1 | 400 | 407 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 97 | 107 | PF00244 | 0.546 |
LIG_APCC_ABBA_1 | 243 | 248 | PF00400 | 0.460 |
LIG_BIR_III_2 | 132 | 136 | PF00653 | 0.671 |
LIG_BRCT_BRCA1_1 | 532 | 536 | PF00533 | 0.438 |
LIG_eIF4E_1 | 259 | 265 | PF01652 | 0.420 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.460 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.511 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.736 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.571 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 219 | 227 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 355 | 365 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 450 | 460 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 58 | 68 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 450 | 456 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 541 | 547 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.700 |
LIG_NRBOX | 162 | 168 | PF00104 | 0.526 |
LIG_PCNA_yPIPBox_3 | 256 | 265 | PF02747 | 0.411 |
LIG_PDZ_Class_1 | 555 | 560 | PF00595 | 0.438 |
LIG_REV1ctd_RIR_1 | 355 | 364 | PF16727 | 0.662 |
LIG_RPA_C_Fungi | 465 | 477 | PF08784 | 0.576 |
LIG_SH2_GRB2like | 34 | 37 | PF00017 | 0.614 |
LIG_SH2_STAP1 | 189 | 193 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 453 | 457 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.641 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.724 |
LIG_SUMO_SIM_anti_2 | 151 | 157 | PF11976 | 0.519 |
LIG_SUMO_SIM_anti_2 | 378 | 385 | PF11976 | 0.629 |
LIG_SUMO_SIM_anti_2 | 84 | 93 | PF11976 | 0.624 |
LIG_SUMO_SIM_par_1 | 166 | 172 | PF11976 | 0.372 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.607 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.409 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.715 |
LIG_TRAF2_1 | 483 | 486 | PF00917 | 0.700 |
LIG_UBA3_1 | 163 | 171 | PF00899 | 0.424 |
LIG_UBA3_1 | 383 | 392 | PF00899 | 0.614 |
LIG_WRC_WIRS_1 | 200 | 205 | PF05994 | 0.438 |
MOD_CDK_SPxxK_3 | 191 | 198 | PF00069 | 0.372 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.530 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.448 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.458 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.710 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.535 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.649 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.605 |
MOD_Cter_Amidation | 227 | 230 | PF01082 | 0.321 |
MOD_Cter_Amidation | 493 | 496 | PF01082 | 0.445 |
MOD_Cter_Amidation | 7 | 10 | PF01082 | 0.706 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.480 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.682 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.536 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.610 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.652 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.413 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.501 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.566 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.521 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.739 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.775 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.438 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.631 |
MOD_N-GLC_2 | 43 | 45 | PF02516 | 0.665 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.306 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.306 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.306 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.399 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.690 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.633 |
MOD_PIKK_1 | 528 | 534 | PF00454 | 0.396 |
MOD_PKA_1 | 124 | 130 | PF00069 | 0.667 |
MOD_PKA_1 | 330 | 336 | PF00069 | 0.644 |
MOD_PKA_1 | 47 | 53 | PF00069 | 0.744 |
MOD_PKA_1 | 9 | 15 | PF00069 | 0.757 |
MOD_PKA_1 | 97 | 103 | PF00069 | 0.570 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.796 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.650 |
MOD_Plk_2-3 | 379 | 385 | PF00069 | 0.641 |
MOD_Plk_2-3 | 446 | 452 | PF00069 | 0.698 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.440 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.438 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.306 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.547 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.427 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.372 |
MOD_SUMO_for_1 | 156 | 159 | PF00179 | 0.565 |
MOD_SUMO_for_1 | 224 | 227 | PF00179 | 0.306 |
MOD_SUMO_for_1 | 538 | 541 | PF00179 | 0.442 |
MOD_SUMO_rev_2 | 186 | 194 | PF00179 | 0.417 |
MOD_SUMO_rev_2 | 202 | 208 | PF00179 | 0.407 |
MOD_SUMO_rev_2 | 248 | 257 | PF00179 | 0.397 |
TRG_DiLeu_BaEn_1 | 159 | 164 | PF01217 | 0.452 |
TRG_DiLeu_BaEn_1 | 379 | 384 | PF01217 | 0.643 |
TRG_DiLeu_BaLyEn_6 | 260 | 265 | PF01217 | 0.416 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.540 |
TRG_ER_diArg_1 | 387 | 390 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 481 | 483 | PF00400 | 0.753 |
TRG_ER_diArg_1 | 505 | 508 | PF00400 | 0.442 |
TRG_NLS_MonoExtC_3 | 8 | 13 | PF00514 | 0.680 |
TRG_NLS_MonoExtC_3 | 96 | 102 | PF00514 | 0.607 |
TRG_NLS_MonoExtN_4 | 6 | 13 | PF00514 | 0.675 |
TRG_NLS_MonoExtN_4 | 94 | 101 | PF00514 | 0.604 |
TRG_PTS1 | 557 | 560 | PF00515 | 0.438 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDH2 | Leptomonas seymouri | 74% | 100% |
A0A0S4JBP1 | Bodo saltans | 40% | 100% |
A0A1X0NYI2 | Trypanosomatidae | 49% | 100% |
A0A422P1Q1 | Trypanosoma rangeli | 50% | 100% |
A4HGB3 | Leishmania braziliensis | 85% | 98% |
A4I3E7 | Leishmania infantum | 100% | 100% |
D0A800 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9AZN4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q8J7 | Leishmania major | 97% | 100% |
V5BG83 | Trypanosoma cruzi | 49% | 100% |