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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: E9B4T5
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0016491 | oxidoreductase activity | 2 | 16 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 16 |
GO:0017150 | tRNA dihydrouridine synthase activity | 5 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0106413 | dihydrouridine synthase activity | 4 | 16 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 16 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 16 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 403 | 407 | PF00656 | 0.622 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.609 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.241 |
DEG_APCC_DBOX_1 | 461 | 469 | PF00400 | 0.416 |
DOC_CYCLIN_yCln2_LP_2 | 301 | 307 | PF00134 | 0.490 |
DOC_CYCLIN_yCln2_LP_2 | 336 | 342 | PF00134 | 0.435 |
DOC_MAPK_gen_1 | 295 | 305 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 298 | 307 | PF00069 | 0.426 |
DOC_PP1_RVXF_1 | 256 | 263 | PF00149 | 0.436 |
DOC_PP1_RVXF_1 | 390 | 397 | PF00149 | 0.619 |
DOC_PP2B_LxvP_1 | 301 | 304 | PF13499 | 0.490 |
DOC_PP2B_LxvP_1 | 397 | 400 | PF13499 | 0.663 |
DOC_PP2B_LxvP_1 | 440 | 443 | PF13499 | 0.490 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.321 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.513 |
DOC_USP7_MATH_2 | 424 | 430 | PF00917 | 0.304 |
DOC_USP7_UBL2_3 | 249 | 253 | PF12436 | 0.547 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.733 |
LIG_14-3-3_CanoR_1 | 121 | 129 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 257 | 261 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 364 | 374 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 392 | 397 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 411 | 415 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 469 | 475 | PF00244 | 0.392 |
LIG_Actin_WH2_2 | 241 | 259 | PF00022 | 0.450 |
LIG_Actin_WH2_2 | 307 | 325 | PF00022 | 0.531 |
LIG_AP2alpha_1 | 384 | 388 | PF02296 | 0.440 |
LIG_APCC_ABBA_1 | 172 | 177 | PF00400 | 0.448 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.634 |
LIG_BRCT_BRCA1_1 | 258 | 262 | PF00533 | 0.438 |
LIG_BRCT_BRCA1_1 | 384 | 388 | PF00533 | 0.551 |
LIG_eIF4E_1 | 93 | 99 | PF01652 | 0.427 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.465 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.532 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.664 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.472 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.543 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.518 |
LIG_GBD_Chelix_1 | 209 | 217 | PF00786 | 0.171 |
LIG_LIR_Apic_2 | 359 | 365 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 123 | 130 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 272 | 281 | PF02991 | 0.531 |
LIG_LIR_LC3C_4 | 150 | 155 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 143 | 147 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 272 | 276 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.395 |
LIG_Pex14_1 | 89 | 93 | PF04695 | 0.487 |
LIG_Pex14_2 | 384 | 388 | PF04695 | 0.551 |
LIG_SH2_CRK | 93 | 97 | PF00017 | 0.363 |
LIG_SH2_NCK_1 | 412 | 416 | PF00017 | 0.542 |
LIG_SH2_PTP2 | 456 | 459 | PF00017 | 0.368 |
LIG_SH2_SRC | 484 | 487 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 8 | 12 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.464 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.555 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.434 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.450 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.770 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.602 |
LIG_SUMO_SIM_anti_2 | 470 | 476 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 39 | 44 | PF11976 | 0.472 |
LIG_TRAF2_1 | 477 | 480 | PF00917 | 0.381 |
LIG_TRAF2_1 | 66 | 69 | PF00917 | 0.486 |
LIG_WW_3 | 364 | 368 | PF00397 | 0.541 |
MOD_CDC14_SPxK_1 | 389 | 392 | PF00782 | 0.484 |
MOD_CDK_SPK_2 | 420 | 425 | PF00069 | 0.503 |
MOD_CDK_SPxK_1 | 386 | 392 | PF00069 | 0.490 |
MOD_CDK_SPxxK_3 | 133 | 140 | PF00069 | 0.531 |
MOD_CDK_SPxxK_3 | 455 | 462 | PF00069 | 0.340 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.406 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.538 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.669 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.335 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.727 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.506 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.532 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.557 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.342 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.535 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.525 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.251 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.248 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.272 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.243 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.552 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.612 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.441 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.470 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.460 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.458 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.450 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.628 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.617 |
MOD_LATS_1 | 277 | 283 | PF00433 | 0.490 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.386 |
MOD_N-GLC_1 | 470 | 475 | PF02516 | 0.452 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.444 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.660 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.597 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.351 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.616 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.472 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.396 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.449 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.521 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.445 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.573 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.450 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.595 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.473 |
MOD_Plk_1 | 470 | 476 | PF00069 | 0.380 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.531 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.405 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.536 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.705 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.402 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.548 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.449 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.720 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.581 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.668 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.539 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.388 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.736 |
TRG_DiLeu_BaEn_1 | 292 | 297 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.318 |
TRG_ER_diArg_1 | 256 | 258 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 362 | 364 | PF00400 | 0.487 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBT7 | Leptomonas seymouri | 62% | 96% |
A0A0S4JTG4 | Bodo saltans | 45% | 100% |
A0A1X0PAA8 | Trypanosomatidae | 45% | 100% |
A0A3Q8IJ00 | Leishmania donovani | 24% | 100% |
A0A3Q8IN46 | Leishmania donovani | 92% | 100% |
A0A3R7KZP3 | Trypanosoma rangeli | 44% | 100% |
A4HAN2 | Leishmania braziliensis | 80% | 100% |
A4HNQ5 | Leishmania braziliensis | 24% | 100% |
A4I9S4 | Leishmania infantum | 92% | 100% |
A4ICU0 | Leishmania infantum | 24% | 100% |
C9ZMV8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9ASG4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4Q391 | Leishmania major | 93% | 100% |
V5DJT2 | Trypanosoma cruzi | 45% | 100% |