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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HFA5
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 9 |
GO:0016491 | oxidoreductase activity | 2 | 8 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 9 |
GO:0071949 | FAD binding | 5 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0004497 | monooxygenase activity | 3 | 4 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 1 |
GO:0016709 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen | 4 | 1 |
GO:0018658 | salicylate 1-monooxygenase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.418 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.233 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.418 |
CLV_PCSK_PC7_1 | 143 | 149 | PF00082 | 0.376 |
CLV_PCSK_PC7_1 | 325 | 331 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.330 |
DEG_APCC_DBOX_1 | 411 | 419 | PF00400 | 0.465 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.260 |
DEG_SPOP_SBC_1 | 207 | 211 | PF00917 | 0.444 |
DOC_CDC14_PxL_1 | 29 | 37 | PF14671 | 0.320 |
DOC_CYCLIN_RxL_1 | 195 | 205 | PF00134 | 0.275 |
DOC_CYCLIN_RxL_1 | 285 | 294 | PF00134 | 0.289 |
DOC_CYCLIN_yCln2_LP_2 | 318 | 324 | PF00134 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 418 | 424 | PF00134 | 0.498 |
DOC_MAPK_DCC_7 | 147 | 155 | PF00069 | 0.376 |
DOC_MAPK_gen_1 | 147 | 155 | PF00069 | 0.320 |
DOC_MAPK_gen_1 | 241 | 250 | PF00069 | 0.274 |
DOC_MAPK_MEF2A_6 | 147 | 155 | PF00069 | 0.376 |
DOC_MAPK_MEF2A_6 | 417 | 426 | PF00069 | 0.442 |
DOC_PP2B_LxvP_1 | 311 | 314 | PF13499 | 0.398 |
DOC_PP2B_LxvP_1 | 318 | 321 | PF13499 | 0.371 |
DOC_PP2B_LxvP_1 | 365 | 368 | PF13499 | 0.416 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.274 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.344 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.414 |
LIG_14-3-3_CanoR_1 | 134 | 138 | PF00244 | 0.260 |
LIG_14-3-3_CanoR_1 | 241 | 246 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 401 | 407 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 417 | 421 | PF00244 | 0.370 |
LIG_Actin_WH2_2 | 130 | 145 | PF00022 | 0.295 |
LIG_eIF4E_1 | 436 | 442 | PF01652 | 0.345 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.415 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.454 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.501 |
LIG_LIR_Gen_1 | 247 | 258 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.272 |
LIG_PCNA_TLS_4 | 387 | 394 | PF02747 | 0.339 |
LIG_Pex14_2 | 375 | 379 | PF04695 | 0.321 |
LIG_PTB_Apo_2 | 430 | 437 | PF02174 | 0.323 |
LIG_PTB_Phospho_1 | 430 | 436 | PF10480 | 0.321 |
LIG_SH2_PTP2 | 130 | 133 | PF00017 | 0.336 |
LIG_SH2_PTP2 | 39 | 42 | PF00017 | 0.336 |
LIG_SH2_STAP1 | 43 | 47 | PF00017 | 0.320 |
LIG_SH2_STAT3 | 393 | 396 | PF00017 | 0.351 |
LIG_SH2_STAT3 | 436 | 439 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.204 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.310 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.405 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.349 |
LIG_WRC_WIRS_1 | 342 | 347 | PF05994 | 0.369 |
MOD_CDK_SPK_2 | 264 | 269 | PF00069 | 0.302 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.260 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.271 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.358 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.387 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.461 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.503 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.404 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.491 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.260 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.336 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.313 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.402 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.474 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.167 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.420 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.461 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.464 |
MOD_N-GLC_1 | 407 | 412 | PF02516 | 0.287 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.342 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.260 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.311 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.521 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.367 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.236 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.320 |
MOD_PIKK_1 | 435 | 441 | PF00454 | 0.443 |
MOD_PKA_1 | 401 | 407 | PF00069 | 0.382 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.376 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.176 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.460 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.369 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.386 |
MOD_PKB_1 | 399 | 407 | PF00069 | 0.382 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.465 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.300 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.279 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.348 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.284 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.376 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.466 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.363 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.320 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.402 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.415 |
MOD_SUMO_rev_2 | 307 | 312 | PF00179 | 0.266 |
MOD_SUMO_rev_2 | 438 | 447 | PF00179 | 0.447 |
TRG_DiLeu_BaEn_1 | 301 | 306 | PF01217 | 0.265 |
TRG_DiLeu_BaEn_2 | 29 | 35 | PF01217 | 0.260 |
TRG_DiLeu_BaLyEn_6 | 196 | 201 | PF01217 | 0.388 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.320 |
TRG_ER_diArg_1 | 146 | 148 | PF00400 | 0.329 |
TRG_ER_diArg_1 | 19 | 21 | PF00400 | 0.233 |
TRG_ER_diArg_1 | 197 | 199 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 398 | 401 | PF00400 | 0.416 |
TRG_NES_CRM1_1 | 273 | 285 | PF08389 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 148 | 152 | PF00026 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 20 | 25 | PF00026 | 0.284 |
TRG_Pf-PMV_PEXEL_1 | 269 | 273 | PF00026 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 392 | 396 | PF00026 | 0.382 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7X9 | Leptomonas seymouri | 81% | 100% |
A0A0S4JHJ1 | Bodo saltans | 23% | 98% |
A0A1B2CTA8 | Penicillium thymicola | 24% | 96% |
A0A1X0P822 | Trypanosomatidae | 64% | 100% |
A0A3Q8IE39 | Leishmania donovani | 87% | 100% |
A1TFU9 | Mycolicibacterium vanbaalenii (strain DSM 7251 / JCM 13017 / BCRC 16820 / KCTC 9966 / NRRL B-24157 / PYR-1) | 24% | 100% |
A4I2I2 | Leishmania infantum | 88% | 100% |
C9ZWZ8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9AYP2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q02N79 | Pseudomonas aeruginosa (strain UCBPP-PA14) | 26% | 100% |
Q0JCU7 | Oryza sativa subsp. japonica | 24% | 69% |
Q4Q8T0 | Leishmania major | 87% | 100% |
Q5EXK1 | Klebsiella oxytoca | 24% | 100% |
Q6F6Y2 | Acinetobacter baylyi (strain ATCC 33305 / BD413 / ADP1) | 24% | 100% |
Q9I0Q0 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 27% | 100% |
V5BGR2 | Trypanosoma cruzi | 65% | 100% |