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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
Related structures:
AlphaFold database: A4HAN2
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 15 |
GO:0003824 | catalytic activity | 1 | 15 |
GO:0005488 | binding | 1 | 15 |
GO:0016491 | oxidoreductase activity | 2 | 15 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 15 |
GO:0017150 | tRNA dihydrouridine synthase activity | 5 | 15 |
GO:0036094 | small molecule binding | 2 | 15 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043168 | anion binding | 3 | 15 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:0106413 | dihydrouridine synthase activity | 4 | 15 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 15 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 15 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 15 |
GO:1901265 | nucleoside phosphate binding | 3 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 180 | 184 | PF00656 | 0.382 |
CLV_C14_Caspase3-7 | 422 | 426 | PF00656 | 0.540 |
CLV_C14_Caspase3-7 | 86 | 90 | PF00656 | 0.502 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.174 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.575 |
DEG_APCC_DBOX_1 | 480 | 488 | PF00400 | 0.410 |
DEG_Kelch_actinfilin_1 | 242 | 246 | PF01344 | 0.403 |
DOC_CYCLIN_yCln2_LP_2 | 320 | 326 | PF00134 | 0.488 |
DOC_CYCLIN_yCln2_LP_2 | 355 | 361 | PF00134 | 0.434 |
DOC_MAPK_DCC_7 | 405 | 415 | PF00069 | 0.369 |
DOC_MAPK_gen_1 | 314 | 324 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 317 | 326 | PF00069 | 0.424 |
DOC_PP1_RVXF_1 | 409 | 416 | PF00149 | 0.521 |
DOC_PP2B_LxvP_1 | 320 | 323 | PF13499 | 0.488 |
DOC_PP2B_LxvP_1 | 416 | 419 | PF13499 | 0.508 |
DOC_PP2B_LxvP_1 | 459 | 462 | PF13499 | 0.479 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.510 |
DOC_USP7_MATH_2 | 443 | 449 | PF00917 | 0.300 |
DOC_USP7_UBL2_3 | 268 | 272 | PF12436 | 0.543 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.374 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.712 |
LIG_14-3-3_CanoR_1 | 140 | 148 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 298 | 304 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 411 | 416 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 421 | 429 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 430 | 434 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 488 | 494 | PF00244 | 0.386 |
LIG_Actin_WH2_2 | 260 | 278 | PF00022 | 0.450 |
LIG_Actin_WH2_2 | 326 | 344 | PF00022 | 0.529 |
LIG_APCC_ABBA_1 | 191 | 196 | PF00400 | 0.446 |
LIG_APCC_ABBA_1 | 500 | 505 | PF00400 | 0.293 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.279 |
LIG_BRCT_BRCA1_1 | 277 | 281 | PF00533 | 0.434 |
LIG_BRCT_BRCA1_1 | 403 | 407 | PF00533 | 0.510 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.461 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.384 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.530 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.605 |
LIG_FHA_2 | 440 | 446 | PF00498 | 0.457 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.557 |
LIG_LIR_Gen_1 | 291 | 300 | PF02991 | 0.529 |
LIG_LIR_LC3C_4 | 169 | 174 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 162 | 166 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 291 | 295 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.571 |
LIG_MYND_1 | 62 | 66 | PF01753 | 0.482 |
LIG_Pex14_1 | 108 | 112 | PF04695 | 0.477 |
LIG_Pex14_2 | 403 | 407 | PF04695 | 0.510 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.368 |
LIG_SH2_NCK_1 | 431 | 435 | PF00017 | 0.491 |
LIG_SH2_PTP2 | 475 | 478 | PF00017 | 0.356 |
LIG_SH2_SRC | 503 | 506 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 143 | 147 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 47 | 51 | PF00017 | 0.593 |
LIG_SH2_STAP1 | 8 | 12 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.337 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.552 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.542 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.450 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.734 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.530 |
LIG_SUMO_SIM_anti_2 | 489 | 496 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 483 | 489 | PF11976 | 0.258 |
LIG_TRAF2_1 | 67 | 70 | PF00917 | 0.533 |
MOD_CDC14_SPxK_1 | 408 | 411 | PF00782 | 0.452 |
MOD_CDK_SPK_2 | 439 | 444 | PF00069 | 0.480 |
MOD_CDK_SPxK_1 | 405 | 411 | PF00069 | 0.451 |
MOD_CDK_SPxxK_3 | 152 | 159 | PF00069 | 0.529 |
MOD_CDK_SPxxK_3 | 474 | 481 | PF00069 | 0.327 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.347 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.380 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.536 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.543 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.601 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.498 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.329 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.530 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.491 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.539 |
MOD_CK2_1 | 474 | 480 | PF00069 | 0.326 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.556 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.249 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.246 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.271 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.241 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.289 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.403 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.441 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.459 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.456 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.527 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.580 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.377 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.340 |
MOD_LATS_1 | 296 | 302 | PF00433 | 0.488 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.383 |
MOD_N-GLC_1 | 41 | 46 | PF02516 | 0.518 |
MOD_N-GLC_1 | 419 | 424 | PF02516 | 0.444 |
MOD_N-GLC_1 | 489 | 494 | PF02516 | 0.445 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.472 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.438 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.373 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.470 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.507 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.528 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.511 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.344 |
MOD_OFUCOSY | 381 | 388 | PF10250 | 0.412 |
MOD_OFUCOSY | 96 | 103 | PF10250 | 0.431 |
MOD_PIKK_1 | 299 | 305 | PF00454 | 0.374 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.669 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.447 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.443 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.441 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.507 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.450 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.489 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.270 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.497 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.373 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.529 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.535 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.323 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.585 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.396 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.545 |
MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.558 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.542 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.521 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.369 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.712 |
TRG_DiLeu_BaEn_1 | 186 | 191 | PF01217 | 0.400 |
TRG_DiLeu_BaEn_1 | 311 | 316 | PF01217 | 0.458 |
TRG_DiLeu_BaEn_1 | 480 | 485 | PF01217 | 0.254 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBT7 | Leptomonas seymouri | 59% | 100% |
A0A0S4JTG4 | Bodo saltans | 44% | 100% |
A0A1X0PAA8 | Trypanosomatidae | 44% | 100% |
A0A3Q8IJ00 | Leishmania donovani | 22% | 100% |
A0A3Q8IN46 | Leishmania donovani | 78% | 100% |
A0A3R7KZP3 | Trypanosoma rangeli | 44% | 100% |
A4HNQ5 | Leishmania braziliensis | 22% | 100% |
A4I9S4 | Leishmania infantum | 78% | 100% |
A4ICU0 | Leishmania infantum | 22% | 100% |
C9ZMV8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9B4T5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q391 | Leishmania major | 79% | 96% |
V5DJT2 | Trypanosoma cruzi | 43% | 100% |