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: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 4 |
GO:0005737 | cytoplasm | 2 | 5 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: Q4QI79
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 5 |
GO:0006259 | DNA metabolic process | 4 | 5 |
GO:0006281 | DNA repair | 5 | 5 |
GO:0006302 | double-strand break repair | 6 | 2 |
GO:0006303 | double-strand break repair via nonhomologous end joining | 7 | 2 |
GO:0006396 | RNA processing | 6 | 5 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0006950 | response to stress | 2 | 5 |
GO:0006974 | DNA damage response | 4 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016070 | RNA metabolic process | 5 | 5 |
GO:0031123 | RNA 3'-end processing | 7 | 5 |
GO:0033554 | cellular response to stress | 3 | 5 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 5 |
GO:0046483 | heterocycle metabolic process | 3 | 5 |
GO:0050896 | response to stimulus | 1 | 5 |
GO:0051716 | cellular response to stimulus | 2 | 5 |
GO:0071076 | RNA 3' uridylation | 8 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:0090304 | nucleic acid metabolic process | 4 | 5 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 5 |
GO:0003677 | DNA binding | 4 | 5 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0003887 | DNA-directed DNA polymerase activity | 5 | 5 |
GO:0005488 | binding | 1 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 5 |
GO:0016779 | nucleotidyltransferase activity | 4 | 5 |
GO:0034061 | DNA polymerase activity | 4 | 5 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043169 | cation binding | 3 | 4 |
GO:0046872 | metal ion binding | 4 | 4 |
GO:0050265 | RNA uridylyltransferase activity | 4 | 5 |
GO:0070569 | uridylyltransferase activity | 5 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 5 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 5 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 5 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 5 |
GO:1901363 | heterocyclic compound binding | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 316 | 320 | PF00656 | 0.477 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.221 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.224 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.208 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 541 | 543 | PF00675 | 0.342 |
CLV_PCSK_FUR_1 | 226 | 230 | PF00082 | 0.473 |
CLV_PCSK_FUR_1 | 489 | 493 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.252 |
CLV_PCSK_PC1ET2_1 | 177 | 179 | PF00082 | 0.394 |
CLV_PCSK_PC1ET2_1 | 217 | 219 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 228 | 230 | PF00082 | 0.344 |
CLV_PCSK_PC7_1 | 224 | 230 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.252 |
DEG_APCC_DBOX_1 | 567 | 575 | PF00400 | 0.477 |
DEG_SCF_TRCP1_1 | 319 | 324 | PF00400 | 0.477 |
DOC_ANK_TNKS_1 | 404 | 411 | PF00023 | 0.377 |
DOC_CYCLIN_RxL_1 | 224 | 236 | PF00134 | 0.475 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 233 | 242 | PF00134 | 0.487 |
DOC_CYCLIN_yCln2_LP_2 | 185 | 188 | PF00134 | 0.444 |
DOC_CYCLIN_yCln2_LP_2 | 423 | 426 | PF00134 | 0.477 |
DOC_MAPK_gen_1 | 224 | 233 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 245 | 253 | PF00069 | 0.334 |
DOC_MAPK_gen_1 | 487 | 495 | PF00069 | 0.434 |
DOC_MAPK_JIP1_4 | 322 | 328 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 247 | 255 | PF00069 | 0.412 |
DOC_PP2B_LxvP_1 | 185 | 188 | PF13499 | 0.444 |
DOC_PP2B_LxvP_1 | 191 | 194 | PF13499 | 0.443 |
DOC_PP2B_LxvP_1 | 423 | 426 | PF13499 | 0.477 |
DOC_PP4_FxxP_1 | 537 | 540 | PF00568 | 0.477 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.638 |
DOC_USP7_UBL2_3 | 177 | 181 | PF12436 | 0.474 |
DOC_USP7_UBL2_3 | 245 | 249 | PF12436 | 0.342 |
DOC_USP7_UBL2_3 | 318 | 322 | PF12436 | 0.485 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.421 |
DOC_USP7_UBL2_3 | 479 | 483 | PF12436 | 0.427 |
DOC_USP7_UBL2_3 | 539 | 543 | PF12436 | 0.477 |
DOC_USP7_UBL2_3 | 621 | 625 | PF12436 | 0.468 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.738 |
LIG_14-3-3_CanoR_1 | 226 | 232 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 459 | 465 | PF00244 | 0.369 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.782 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.642 |
LIG_BIR_III_4 | 606 | 610 | PF00653 | 0.477 |
LIG_BRCT_BRCA1_1 | 499 | 503 | PF00533 | 0.421 |
LIG_BRCT_BRCA1_1 | 512 | 516 | PF00533 | 0.371 |
LIG_EH1_1 | 637 | 645 | PF00400 | 0.377 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.398 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.477 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.377 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.568 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.353 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.377 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.477 |
LIG_FHA_2 | 651 | 657 | PF00498 | 0.477 |
LIG_Integrin_RGD_1 | 178 | 180 | PF01839 | 0.491 |
LIG_LIR_Apic_2 | 664 | 668 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 180 | 191 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 364 | 374 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 378 | 387 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 513 | 524 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 556 | 567 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 656 | 666 | PF02991 | 0.421 |
LIG_LIR_LC3C_4 | 324 | 328 | PF02991 | 0.477 |
LIG_LIR_LC3C_4 | 378 | 383 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 378 | 382 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 513 | 519 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 533 | 537 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 656 | 661 | PF02991 | 0.421 |
LIG_MYND_1 | 188 | 192 | PF01753 | 0.498 |
LIG_MYND_1 | 422 | 426 | PF01753 | 0.477 |
LIG_SH2_CRK | 548 | 552 | PF00017 | 0.477 |
LIG_SH2_PTP2 | 665 | 668 | PF00017 | 0.421 |
LIG_SH2_SRC | 442 | 445 | PF00017 | 0.421 |
LIG_SH2_SRC | 497 | 500 | PF00017 | 0.477 |
LIG_SH2_SRC | 665 | 668 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 379 | 383 | PF00017 | 0.421 |
LIG_SH2_STAT3 | 387 | 390 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 665 | 668 | PF00017 | 0.421 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.575 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.658 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.496 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.622 |
LIG_SH3_4 | 539 | 546 | PF00018 | 0.477 |
LIG_SUMO_SIM_anti_2 | 38 | 44 | PF11976 | 0.375 |
LIG_SUMO_SIM_anti_2 | 396 | 402 | PF11976 | 0.421 |
LIG_TRAF2_1 | 356 | 359 | PF00917 | 0.464 |
LIG_TRAF2_1 | 630 | 633 | PF00917 | 0.477 |
LIG_TRFH_1 | 183 | 187 | PF08558 | 0.449 |
LIG_TRFH_1 | 53 | 57 | PF08558 | 0.633 |
LIG_UBA3_1 | 203 | 209 | PF00899 | 0.423 |
LIG_UBA3_1 | 238 | 245 | PF00899 | 0.471 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.641 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.568 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.450 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.297 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.267 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.320 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.424 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.407 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.384 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.407 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.197 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.337 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.337 |
MOD_CK2_1 | 650 | 656 | PF00069 | 0.337 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.630 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.693 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.741 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.621 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.597 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.528 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.296 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.263 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.248 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.421 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.267 |
MOD_GlcNHglycan | 570 | 574 | PF01048 | 0.295 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.185 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.277 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.352 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.762 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.686 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.453 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.598 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.642 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.434 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.464 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.318 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.417 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.253 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.277 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.337 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.267 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.752 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.610 |
MOD_N-GLC_1 | 582 | 587 | PF02516 | 0.197 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.519 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.337 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.201 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.258 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.337 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.620 |
MOD_NEK2_2 | 555 | 560 | PF00069 | 0.337 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.428 |
MOD_PIKK_1 | 163 | 169 | PF00454 | 0.331 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.258 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.754 |
MOD_PKA_1 | 538 | 544 | PF00069 | 0.337 |
MOD_PKA_1 | 613 | 619 | PF00069 | 0.407 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.332 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.197 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.641 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.258 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.258 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.614 |
MOD_Plk_1 | 555 | 561 | PF00069 | 0.337 |
MOD_Plk_1 | 569 | 575 | PF00069 | 0.148 |
MOD_Plk_2-3 | 21 | 27 | PF00069 | 0.477 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.597 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.738 |
MOD_SUMO_for_1 | 574 | 577 | PF00179 | 0.337 |
MOD_SUMO_rev_2 | 260 | 270 | PF00179 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 419 | 424 | PF01217 | 0.337 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 534 | 537 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 548 | 551 | PF00928 | 0.258 |
TRG_ER_diArg_1 | 369 | 372 | PF00400 | 0.258 |
TRG_ER_diArg_1 | 387 | 389 | PF00400 | 0.258 |
TRG_ER_diArg_1 | 488 | 491 | PF00400 | 0.311 |
TRG_ER_diArg_1 | 646 | 649 | PF00400 | 0.263 |
TRG_NLS_Bipartite_1 | 613 | 628 | PF00514 | 0.337 |
TRG_NLS_MonoExtC_3 | 622 | 627 | PF00514 | 0.316 |
TRG_NLS_MonoExtN_4 | 198 | 203 | PF00514 | 0.504 |
TRG_NLS_MonoExtN_4 | 621 | 628 | PF00514 | 0.330 |
TRG_Pf-PMV_PEXEL_1 | 272 | 276 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 655 | 659 | PF00026 | 0.318 |