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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A0A3Q8IKG6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006351 | DNA-templated transcription | 7 | 3 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009058 | biosynthetic process | 2 | 3 |
GO:0009059 | macromolecule biosynthetic process | 4 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016070 | RNA metabolic process | 5 | 3 |
GO:0018130 | heterocycle biosynthetic process | 4 | 3 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 3 |
GO:0032774 | RNA biosynthetic process | 5 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044249 | cellular biosynthetic process | 3 | 3 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 3 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0090304 | nucleic acid metabolic process | 4 | 3 |
GO:0097659 | nucleic acid-templated transcription | 6 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 3 |
GO:1901576 | organic substance biosynthetic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0008270 | zinc ion binding | 6 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
GO:0046914 | transition metal ion binding | 5 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 394 | 398 | PF00656 | 0.739 |
CLV_C14_Caspase3-7 | 515 | 519 | PF00656 | 0.724 |
CLV_C14_Caspase3-7 | 61 | 65 | PF00656 | 0.515 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.744 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.651 |
CLV_PCSK_FUR_1 | 159 | 163 | PF00082 | 0.729 |
CLV_PCSK_FUR_1 | 168 | 172 | PF00082 | 0.627 |
CLV_PCSK_FUR_1 | 495 | 499 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.715 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.650 |
CLV_PCSK_PC1ET2_1 | 161 | 163 | PF00082 | 0.684 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.653 |
CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.656 |
CLV_PCSK_PC7_1 | 168 | 174 | PF00082 | 0.595 |
CLV_PCSK_PC7_1 | 493 | 499 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.709 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.504 |
DEG_SCF_FBW7_1 | 113 | 120 | PF00400 | 0.834 |
DOC_CKS1_1 | 114 | 119 | PF01111 | 0.699 |
DOC_CKS1_1 | 353 | 358 | PF01111 | 0.550 |
DOC_CYCLIN_RxL_1 | 465 | 473 | PF00134 | 0.491 |
DOC_MAPK_DCC_7 | 352 | 361 | PF00069 | 0.542 |
DOC_MAPK_gen_1 | 326 | 335 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 495 | 504 | PF00069 | 0.698 |
DOC_MAPK_MEF2A_6 | 326 | 335 | PF00069 | 0.575 |
DOC_MAPK_MEF2A_6 | 352 | 361 | PF00069 | 0.575 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.561 |
DOC_PP4_FxxP_1 | 506 | 509 | PF00568 | 0.698 |
DOC_PP4_FxxP_1 | 540 | 543 | PF00568 | 0.732 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.598 |
DOC_USP7_UBL2_3 | 163 | 167 | PF12436 | 0.678 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.784 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 525 | 530 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.574 |
LIG_14-3-3_CanoR_1 | 285 | 293 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 326 | 332 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 546 | 555 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 565 | 570 | PF00244 | 0.409 |
LIG_Actin_WH2_2 | 314 | 331 | PF00022 | 0.575 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.710 |
LIG_BIR_III_2 | 105 | 109 | PF00653 | 0.792 |
LIG_BRCT_BRCA1_1 | 536 | 540 | PF00533 | 0.754 |
LIG_CSL_BTD_1 | 23 | 26 | PF09270 | 0.501 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.533 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.560 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.542 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.612 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.481 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.560 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.732 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.734 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.678 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.529 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.676 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.465 |
LIG_LIR_Apic_2 | 505 | 509 | PF02991 | 0.698 |
LIG_LIR_Apic_2 | 537 | 543 | PF02991 | 0.704 |
LIG_LIR_Apic_2 | 549 | 555 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 13 | 22 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 136 | 146 | PF02991 | 0.712 |
LIG_LIR_Nem_3 | 13 | 17 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.716 |
LIG_LIR_Nem_3 | 521 | 527 | PF02991 | 0.799 |
LIG_NRBOX | 466 | 472 | PF00104 | 0.572 |
LIG_PALB2_WD40_1 | 365 | 373 | PF16756 | 0.501 |
LIG_PTB_Apo_2 | 364 | 371 | PF02174 | 0.560 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.662 |
LIG_SH2_CRK | 552 | 556 | PF00017 | 0.525 |
LIG_SH2_STAP1 | 567 | 571 | PF00017 | 0.598 |
LIG_SH2_STAT3 | 249 | 252 | PF00017 | 0.687 |
LIG_SH2_STAT3 | 567 | 570 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.594 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.515 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.668 |
LIG_SUMO_SIM_anti_2 | 43 | 49 | PF11976 | 0.561 |
LIG_SUMO_SIM_par_1 | 450 | 455 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 488 | 494 | PF11976 | 0.555 |
LIG_TRAF2_1 | 107 | 110 | PF00917 | 0.713 |
LIG_TRAF2_1 | 417 | 420 | PF00917 | 0.480 |
LIG_TRAF2_1 | 93 | 96 | PF00917 | 0.525 |
LIG_TRFH_1 | 258 | 262 | PF08558 | 0.759 |
LIG_UBA3_1 | 321 | 329 | PF00899 | 0.492 |
MOD_CDK_SPK_2 | 266 | 271 | PF00069 | 0.680 |
MOD_CDK_SPxxK_3 | 539 | 546 | PF00069 | 0.772 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.707 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.665 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.711 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.629 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.562 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.712 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.751 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.598 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.556 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.762 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.665 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.666 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.499 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.773 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.806 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.757 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.286 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.691 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.718 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.678 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.652 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.660 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.602 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.626 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.501 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.616 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.353 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.362 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.805 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.698 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.663 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.651 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.442 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.528 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.501 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.756 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.667 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.537 |
MOD_LATS_1 | 200 | 206 | PF00433 | 0.594 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.749 |
MOD_N-GLC_1 | 482 | 487 | PF02516 | 0.499 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.729 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.525 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.541 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.566 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.735 |
MOD_OFUCOSY | 390 | 395 | PF10250 | 0.728 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.609 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.501 |
MOD_PIKK_1 | 508 | 514 | PF00454 | 0.709 |
MOD_PK_1 | 565 | 571 | PF00069 | 0.508 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.769 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.664 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.552 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.640 |
MOD_PKA_2 | 545 | 551 | PF00069 | 0.677 |
MOD_PKB_1 | 171 | 179 | PF00069 | 0.600 |
MOD_Plk_1 | 146 | 152 | PF00069 | 0.591 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.525 |
MOD_Plk_2-3 | 222 | 228 | PF00069 | 0.681 |
MOD_Plk_2-3 | 388 | 394 | PF00069 | 0.668 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.366 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.608 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.598 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.785 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.713 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.550 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.671 |
MOD_ProDKin_1 | 525 | 531 | PF00069 | 0.600 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.644 |
MOD_SUMO_for_1 | 247 | 250 | PF00179 | 0.640 |
TRG_DiLeu_BaEn_2 | 298 | 304 | PF01217 | 0.607 |
TRG_DiLeu_BaLyEn_6 | 466 | 471 | PF01217 | 0.575 |
TRG_DiLeu_BaLyEn_6 | 486 | 491 | PF01217 | 0.302 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.662 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.736 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.772 |
TRG_ER_diArg_1 | 467 | 469 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 492 | 495 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 497 | 499 | PF00400 | 0.634 |
TRG_NLS_Bipartite_1 | 159 | 175 | PF00514 | 0.699 |
TRG_NLS_Bipartite_1 | 234 | 249 | PF00514 | 0.695 |
TRG_NLS_MonoCore_2 | 158 | 163 | PF00514 | 0.656 |
TRG_NLS_MonoCore_2 | 166 | 171 | PF00514 | 0.653 |
TRG_NLS_MonoExtC_3 | 158 | 163 | PF00514 | 0.706 |
TRG_NLS_MonoExtC_3 | 166 | 171 | PF00514 | 0.646 |
TRG_NLS_MonoExtC_3 | 188 | 193 | PF00514 | 0.719 |
TRG_NLS_MonoExtC_3 | 244 | 250 | PF00514 | 0.703 |
TRG_NLS_MonoExtN_4 | 159 | 164 | PF00514 | 0.761 |
TRG_NLS_MonoExtN_4 | 166 | 173 | PF00514 | 0.752 |
TRG_NLS_MonoExtN_4 | 188 | 193 | PF00514 | 0.734 |
TRG_NLS_MonoExtN_4 | 242 | 249 | PF00514 | 0.639 |
TRG_Pf-PMV_PEXEL_1 | 468 | 473 | PF00026 | 0.446 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5Y6 | Leptomonas seymouri | 53% | 100% |
A0A1X0NRB1 | Trypanosomatidae | 31% | 100% |
A0A422NKE1 | Trypanosoma rangeli | 33% | 100% |
A4HLZ3 | Leishmania braziliensis | 78% | 99% |
A4I9C3 | Leishmania infantum | 100% | 100% |
E9B4C2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q3Q3 | Leishmania major | 91% | 100% |