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:0001522 | pseudouridine synthesis | 6 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
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:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 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:0000154 | rRNA modification | 6 | 1 |
GO:0000455 | enzyme-directed rRNA pseudouridine synthesis | 8 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0031118 | rRNA pseudouridine synthesis | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0009982 | pseudouridine synthase activity | 4 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016866 | intramolecular transferase activity | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0106029 | tRNA pseudouridine synthase activity | 5 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.487 |
CLV_PCSK_FUR_1 | 147 | 151 | PF00082 | 0.454 |
CLV_PCSK_FUR_1 | 96 | 100 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.386 |
CLV_PCSK_PC1ET2_1 | 243 | 245 | PF00082 | 0.255 |
CLV_PCSK_PC1ET2_1 | 398 | 400 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 86 | 88 | PF00082 | 0.464 |
CLV_PCSK_PC7_1 | 239 | 245 | PF00082 | 0.255 |
CLV_PCSK_PC7_1 | 3 | 9 | PF00082 | 0.597 |
CLV_PCSK_PC7_1 | 98 | 104 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.415 |
DEG_COP1_1 | 113 | 123 | PF00400 | 0.441 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.722 |
DOC_CYCLIN_yCln2_LP_2 | 199 | 205 | PF00134 | 0.541 |
DOC_CYCLIN_yCln2_LP_2 | 400 | 406 | PF00134 | 0.561 |
DOC_MAPK_gen_1 | 102 | 114 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 32 | 42 | PF00069 | 0.598 |
DOC_MAPK_gen_1 | 359 | 366 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 34 | 42 | PF00069 | 0.613 |
DOC_MAPK_MEF2A_6 | 359 | 366 | PF00069 | 0.497 |
DOC_MAPK_NFAT4_5 | 35 | 43 | PF00069 | 0.627 |
DOC_PP1_RVXF_1 | 109 | 115 | PF00149 | 0.408 |
DOC_PP1_RVXF_1 | 396 | 403 | PF00149 | 0.407 |
DOC_PP2B_LxvP_1 | 130 | 133 | PF13499 | 0.489 |
DOC_PP2B_LxvP_1 | 331 | 334 | PF13499 | 0.488 |
DOC_PP4_FxxP_1 | 354 | 357 | PF00568 | 0.384 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.395 |
LIG_14-3-3_CanoR_1 | 107 | 114 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 2 | 7 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 204 | 213 | PF00244 | 0.560 |
LIG_APCC_ABBA_1 | 266 | 271 | PF00400 | 0.455 |
LIG_APCC_ABBA_1 | 351 | 356 | PF00400 | 0.399 |
LIG_APCC_ABBAyCdc20_2 | 265 | 271 | PF00400 | 0.455 |
LIG_EVH1_2 | 259 | 263 | PF00568 | 0.541 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.406 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.489 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.367 |
LIG_G3BP_FGDF_1 | 305 | 310 | PF02136 | 0.480 |
LIG_GBD_Chelix_1 | 192 | 200 | PF00786 | 0.341 |
LIG_LIR_Apic_2 | 352 | 357 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 309 | 316 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 54 | 65 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 79 | 89 | PF02991 | 0.401 |
LIG_LIR_LC3C_4 | 115 | 119 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 306 | 310 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 312 | 316 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.471 |
LIG_Pex14_1 | 10 | 14 | PF04695 | 0.639 |
LIG_PTB_Apo_2 | 245 | 252 | PF02174 | 0.455 |
LIG_PTB_Phospho_1 | 245 | 251 | PF10480 | 0.455 |
LIG_SH2_CRK | 105 | 109 | PF00017 | 0.471 |
LIG_SH2_CRK | 57 | 61 | PF00017 | 0.518 |
LIG_SH2_GRB2like | 205 | 208 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.466 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.401 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.455 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.455 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.480 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.376 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.412 |
LIG_SH3_5 | 78 | 82 | PF00018 | 0.520 |
LIG_SUMO_SIM_anti_2 | 115 | 122 | PF11976 | 0.368 |
LIG_SUMO_SIM_anti_2 | 172 | 178 | PF11976 | 0.307 |
LIG_SUMO_SIM_par_1 | 115 | 122 | PF11976 | 0.368 |
LIG_TRAF2_1 | 44 | 47 | PF00917 | 0.558 |
LIG_TYR_ITIM | 55 | 60 | PF00017 | 0.415 |
LIG_UBA3_1 | 236 | 243 | PF00899 | 0.307 |
LIG_Vh1_VBS_1 | 210 | 228 | PF01044 | 0.202 |
LIG_WRC_WIRS_1 | 307 | 312 | PF05994 | 0.302 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.691 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.323 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.527 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.533 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.668 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.323 |
MOD_Cter_Amidation | 100 | 103 | PF01082 | 0.469 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.496 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.516 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.392 |
MOD_GlcNHglycan | 220 | 224 | PF01048 | 0.323 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.305 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.323 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.394 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.638 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.364 |
MOD_N-GLC_1 | 300 | 305 | PF02516 | 0.323 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.618 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.316 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.307 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.380 |
MOD_PIKK_1 | 141 | 147 | PF00454 | 0.680 |
MOD_PIKK_1 | 205 | 211 | PF00454 | 0.454 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.419 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.407 |
MOD_PKA_1 | 103 | 109 | PF00069 | 0.416 |
MOD_PKA_1 | 2 | 8 | PF00069 | 0.464 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.423 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.464 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.449 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.549 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.323 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.404 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.548 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.474 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.323 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.302 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.405 |
MOD_SUMO_for_1 | 169 | 172 | PF00179 | 0.398 |
TRG_DiLeu_BaEn_1 | 113 | 118 | PF01217 | 0.390 |
TRG_DiLeu_BaEn_2 | 305 | 311 | PF01217 | 0.307 |
TRG_DiLeu_BaLyEn_6 | 331 | 336 | PF01217 | 0.392 |
TRG_DiLeu_BaLyEn_6 | 406 | 411 | PF01217 | 0.397 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.400 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 103 | 105 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 265 | 268 | PF00400 | 0.307 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.473 |
TRG_NLS_Bipartite_1 | 86 | 106 | PF00514 | 0.450 |
TRG_NLS_MonoExtN_4 | 99 | 106 | PF00514 | 0.453 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I599 | Leptomonas seymouri | 85% | 100% |
A0A0S4J1Y1 | Bodo saltans | 67% | 100% |
A0A1X0P2Q5 | Trypanosomatidae | 71% | 100% |
A0A3S5H4U1 | Leishmania donovani | 93% | 100% |
A0A422NY76 | Trypanosoma rangeli | 74% | 100% |
A4HRE9 | Leishmania infantum | 93% | 100% |
C9ZXE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 71% | 100% |
E9AC17 | Leishmania major | 93% | 100% |
E9AJB4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
P0AA39 | Escherichia coli (strain K12) | 22% | 100% |
P0AA40 | Shigella flexneri | 22% | 100% |
P44433 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 23% | 100% |
P59835 | Haemophilus ducreyi (strain 35000HP / ATCC 700724) | 24% | 100% |
P74346 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 24% | 100% |
Q28C59 | Xenopus tropicalis | 27% | 100% |
Q4QQT0 | Rattus norvegicus | 26% | 100% |
Q5E9Z1 | Bos taurus | 25% | 100% |
Q6DBR0 | Danio rerio | 27% | 100% |
Q87N15 | Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633) | 22% | 100% |
Q89AH2 | Buchnera aphidicola subsp. Baizongia pistaciae (strain Bp) | 21% | 100% |
Q8D8G1 | Vibrio vulnificus (strain CMCP6) | 21% | 100% |
Q8FIP7 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) | 22% | 100% |
Q8X8J3 | Escherichia coli O157:H7 | 22% | 100% |
Q8Z7J7 | Salmonella typhi | 22% | 100% |
Q8ZQ16 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 22% | 100% |
Q96CM3 | Homo sapiens | 25% | 100% |
Q9CM51 | Pasteurella multocida (strain Pm70) | 22% | 100% |
Q9CWX4 | Mus musculus | 26% | 100% |
Q9HZM9 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 21% | 100% |
Q9KQH0 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 22% | 100% |
Q9LT72 | Arabidopsis thaliana | 25% | 87% |
V5B9Z1 | Trypanosoma cruzi | 72% | 100% |