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:0005654 | nucleoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H9R8
Term | Name | Level | Count |
---|---|---|---|
GO:0006518 | peptide metabolic process | 4 | 12 |
GO:0006575 | cellular modified amino acid metabolic process | 3 | 12 |
GO:0006749 | glutathione metabolic process | 4 | 12 |
GO:0006750 | glutathione biosynthetic process | 5 | 12 |
GO:0006790 | sulfur compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0019184 | nonribosomal peptide biosynthetic process | 6 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0042398 | cellular modified amino acid biosynthetic process | 4 | 12 |
GO:0043043 | peptide biosynthetic process | 5 | 12 |
GO:0043603 | amide metabolic process | 3 | 12 |
GO:0043604 | amide biosynthetic process | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 12 |
GO:0044272 | sulfur compound biosynthetic process | 4 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004357 | glutamate-cysteine ligase activity | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 12 |
GO:0016881 | acid-amino acid ligase activity | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 115 | 119 | PF00656 | 0.390 |
CLV_C14_Caspase3-7 | 414 | 418 | PF00656 | 0.373 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.294 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.330 |
CLV_PCSK_FUR_1 | 187 | 191 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 643 | 645 | PF00082 | 0.341 |
CLV_PCSK_PC1ET2_1 | 605 | 607 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 643 | 645 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 559 | 563 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 634 | 638 | PF00082 | 0.328 |
DEG_COP1_1 | 162 | 170 | PF00400 | 0.313 |
DEG_SPOP_SBC_1 | 243 | 247 | PF00917 | 0.501 |
DOC_CKS1_1 | 274 | 279 | PF01111 | 0.372 |
DOC_CKS1_1 | 504 | 509 | PF01111 | 0.234 |
DOC_CYCLIN_RxL_1 | 269 | 279 | PF00134 | 0.533 |
DOC_CYCLIN_RxL_1 | 362 | 372 | PF00134 | 0.328 |
DOC_CYCLIN_yCln2_LP_2 | 274 | 280 | PF00134 | 0.417 |
DOC_MAPK_DCC_7 | 192 | 202 | PF00069 | 0.363 |
DOC_MAPK_gen_1 | 187 | 196 | PF00069 | 0.295 |
DOC_MAPK_gen_1 | 395 | 403 | PF00069 | 0.268 |
DOC_MAPK_gen_1 | 40 | 48 | PF00069 | 0.461 |
DOC_MAPK_gen_1 | 438 | 448 | PF00069 | 0.168 |
DOC_MAPK_GRA24_9 | 186 | 202 | PF00069 | 0.364 |
DOC_MAPK_HePTP_8 | 186 | 198 | PF00069 | 0.295 |
DOC_MAPK_MEF2A_6 | 189 | 198 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 397 | 405 | PF00069 | 0.268 |
DOC_PP1_RVXF_1 | 493 | 499 | PF00149 | 0.234 |
DOC_PP1_RVXF_1 | 526 | 532 | PF00149 | 0.157 |
DOC_PP2B_LxvP_1 | 165 | 168 | PF13499 | 0.317 |
DOC_PP4_FxxP_1 | 483 | 486 | PF00568 | 0.328 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.286 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.234 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.298 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.343 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.234 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.234 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.438 |
LIG_14-3-3_CanoR_1 | 235 | 242 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 298 | 304 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 615 | 620 | PF00244 | 0.225 |
LIG_14-3-3_CanoR_1 | 633 | 642 | PF00244 | 0.332 |
LIG_Actin_WH2_2 | 175 | 191 | PF00022 | 0.308 |
LIG_APCC_ABBA_1 | 198 | 203 | PF00400 | 0.309 |
LIG_BRCT_BRCA1_1 | 479 | 483 | PF00533 | 0.157 |
LIG_deltaCOP1_diTrp_1 | 491 | 498 | PF00928 | 0.293 |
LIG_eIF4E_1 | 590 | 596 | PF01652 | 0.249 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.292 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.281 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.249 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.389 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.268 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.453 |
LIG_FHA_1 | 663 | 669 | PF00498 | 0.342 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.442 |
LIG_FHA_2 | 463 | 469 | PF00498 | 0.249 |
LIG_FHA_2 | 504 | 510 | PF00498 | 0.234 |
LIG_FHA_2 | 565 | 571 | PF00498 | 0.293 |
LIG_FHA_2 | 575 | 581 | PF00498 | 0.204 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.420 |
LIG_LIR_Apic_2 | 302 | 307 | PF02991 | 0.340 |
LIG_LIR_Apic_2 | 480 | 486 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 121 | 132 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 138 | 146 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 372 | 382 | PF02991 | 0.234 |
LIG_LIR_Gen_1 | 396 | 405 | PF02991 | 0.243 |
LIG_LIR_Gen_1 | 425 | 433 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 475 | 486 | PF02991 | 0.234 |
LIG_LIR_Gen_1 | 612 | 621 | PF02991 | 0.238 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 396 | 401 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 425 | 429 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 468 | 473 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 475 | 481 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 586 | 592 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 612 | 616 | PF02991 | 0.238 |
LIG_LIR_Nem_3 | 92 | 96 | PF02991 | 0.313 |
LIG_PDZ_Class_1 | 683 | 688 | PF00595 | 0.434 |
LIG_Pex14_1 | 494 | 498 | PF04695 | 0.234 |
LIG_Pex14_1 | 89 | 93 | PF04695 | 0.316 |
LIG_Pex14_2 | 33 | 37 | PF04695 | 0.405 |
LIG_PTB_Apo_2 | 507 | 514 | PF02174 | 0.237 |
LIG_PTB_Apo_2 | 87 | 94 | PF02174 | 0.349 |
LIG_PTB_Phospho_1 | 87 | 93 | PF10480 | 0.351 |
LIG_SH2_CRK | 124 | 128 | PF00017 | 0.366 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.333 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.234 |
LIG_SH2_CRK | 398 | 402 | PF00017 | 0.268 |
LIG_SH2_CRK | 532 | 536 | PF00017 | 0.286 |
LIG_SH2_CRK | 590 | 594 | PF00017 | 0.249 |
LIG_SH2_NCK_1 | 398 | 402 | PF00017 | 0.281 |
LIG_SH2_NCK_1 | 532 | 536 | PF00017 | 0.299 |
LIG_SH2_SRC | 599 | 602 | PF00017 | 0.178 |
LIG_SH2_STAP1 | 161 | 165 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 283 | 287 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 344 | 348 | PF00017 | 0.293 |
LIG_SH2_STAP1 | 455 | 459 | PF00017 | 0.268 |
LIG_SH2_STAT3 | 282 | 285 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.157 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.234 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.234 |
LIG_SH2_STAT5 | 599 | 602 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.123 |
LIG_SH2_STAT5 | 673 | 676 | PF00017 | 0.394 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.278 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.382 |
LIG_SH3_3 | 512 | 518 | PF00018 | 0.328 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.270 |
LIG_SUMO_SIM_anti_2 | 345 | 351 | PF11976 | 0.328 |
LIG_SUMO_SIM_anti_2 | 533 | 540 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 456 | 463 | PF11976 | 0.245 |
LIG_SUMO_SIM_par_1 | 63 | 69 | PF11976 | 0.457 |
LIG_TRAF2_1 | 260 | 263 | PF00917 | 0.502 |
LIG_TRFH_1 | 590 | 594 | PF08558 | 0.249 |
LIG_WRC_WIRS_1 | 676 | 681 | PF05994 | 0.269 |
LIG_WRC_WIRS_1 | 93 | 98 | PF05994 | 0.310 |
MOD_CDK_SPxxK_3 | 358 | 365 | PF00069 | 0.234 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.337 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.324 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.256 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.214 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.305 |
MOD_CK2_1 | 503 | 509 | PF00069 | 0.234 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.302 |
MOD_CK2_1 | 574 | 580 | PF00069 | 0.207 |
MOD_CK2_1 | 674 | 680 | PF00069 | 0.293 |
MOD_Cter_Amidation | 190 | 193 | PF01082 | 0.246 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.272 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.299 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.293 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.342 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.389 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.317 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.291 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.207 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.373 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.481 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.364 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.252 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.203 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.280 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.292 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.399 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.277 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.323 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.270 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.670 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.553 |
MOD_N-GLC_1 | 422 | 427 | PF02516 | 0.258 |
MOD_N-GLC_2 | 564 | 566 | PF02516 | 0.178 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.397 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.249 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.234 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.210 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.276 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.222 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.295 |
MOD_NEK2_2 | 161 | 166 | PF00069 | 0.344 |
MOD_NEK2_2 | 267 | 272 | PF00069 | 0.387 |
MOD_NEK2_2 | 299 | 304 | PF00069 | 0.359 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.415 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.379 |
MOD_PK_1 | 305 | 311 | PF00069 | 0.315 |
MOD_PK_1 | 397 | 403 | PF00069 | 0.268 |
MOD_PKA_1 | 643 | 649 | PF00069 | 0.157 |
MOD_PKA_2 | 619 | 625 | PF00069 | 0.293 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.271 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.271 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.206 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.372 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.546 |
MOD_Plk_1 | 422 | 428 | PF00069 | 0.254 |
MOD_Plk_1 | 462 | 468 | PF00069 | 0.263 |
MOD_Plk_1 | 574 | 580 | PF00069 | 0.183 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.381 |
MOD_Plk_2-3 | 203 | 209 | PF00069 | 0.389 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.301 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.340 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.576 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.383 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.312 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.335 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.509 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.463 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.361 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.234 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.234 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.379 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.448 |
MOD_SUMO_rev_2 | 601 | 607 | PF00179 | 0.288 |
TRG_DiLeu_BaEn_2 | 91 | 97 | PF01217 | 0.315 |
TRG_DiLeu_BaLyEn_6 | 515 | 520 | PF01217 | 0.328 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.234 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.248 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.234 |
TRG_ENDOCYTIC_2 | 673 | 676 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.310 |
TRG_ER_diArg_1 | 186 | 189 | PF00400 | 0.275 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.371 |
TRG_Pf-PMV_PEXEL_1 | 385 | 389 | PF00026 | 0.145 |
TRG_Pf-PMV_PEXEL_1 | 598 | 603 | PF00026 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 654 | 658 | PF00026 | 0.299 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9N5 | Leptomonas seymouri | 71% | 100% |
A0A0S4IM75 | Bodo saltans | 53% | 100% |
A0A1X0P757 | Trypanosomatidae | 58% | 100% |
A0A3S5IRL4 | Trypanosoma rangeli | 59% | 100% |
A0A3S7WV51 | Leishmania donovani | 77% | 100% |
A4HY37 | Leishmania infantum | 77% | 100% |
D0A548 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9ARV1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
P32477 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 100% |
Q09768 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
Q4QDM2 | Leishmania major | 77% | 100% |
V5BDE4 | Trypanosoma cruzi | 59% | 100% |