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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HZS9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 179 | 183 | PF00656 | 0.569 |
CLV_C14_Caspase3-7 | 232 | 236 | PF00656 | 0.782 |
CLV_C14_Caspase3-7 | 360 | 364 | PF00656 | 0.589 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.593 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.464 |
DEG_APCC_DBOX_1 | 145 | 153 | PF00400 | 0.623 |
DEG_MDM2_SWIB_1 | 496 | 504 | PF02201 | 0.532 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.522 |
DEG_SCF_TRCP1_1 | 235 | 240 | PF00400 | 0.748 |
DEG_SPOP_SBC_1 | 14 | 18 | PF00917 | 0.592 |
DEG_SPOP_SBC_1 | 265 | 269 | PF00917 | 0.765 |
DEG_SPOP_SBC_1 | 338 | 342 | PF00917 | 0.780 |
DOC_CYCLIN_yCln2_LP_2 | 368 | 374 | PF00134 | 0.626 |
DOC_CYCLIN_yCln2_LP_2 | 492 | 498 | PF00134 | 0.694 |
DOC_MAPK_gen_1 | 217 | 227 | PF00069 | 0.602 |
DOC_MAPK_gen_1 | 314 | 323 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 86 | 93 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 488 | 496 | PF00069 | 0.628 |
DOC_MAPK_RevD_3 | 72 | 87 | PF00069 | 0.576 |
DOC_PP1_RVXF_1 | 53 | 59 | PF00149 | 0.493 |
DOC_PP2B_LxvP_1 | 492 | 495 | PF13499 | 0.683 |
DOC_PP2B_LxvP_1 | 537 | 540 | PF13499 | 0.833 |
DOC_PP2B_LxvP_1 | 59 | 62 | PF13499 | 0.502 |
DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.495 |
DOC_SPAK_OSR1_1 | 71 | 75 | PF12202 | 0.589 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.805 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.727 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.779 |
LIG_14-3-3_CanoR_1 | 115 | 120 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 124 | 130 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 266 | 271 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 287 | 294 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 439 | 448 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 482 | 492 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 529 | 533 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 569 | 576 | PF00244 | 0.599 |
LIG_Actin_WH2_2 | 301 | 319 | PF00022 | 0.590 |
LIG_Actin_WH2_2 | 38 | 54 | PF00022 | 0.581 |
LIG_BIR_III_4 | 363 | 367 | PF00653 | 0.535 |
LIG_BRCT_BRCA1_1 | 229 | 233 | PF00533 | 0.713 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.524 |
LIG_CSL_BTD_1 | 537 | 540 | PF09270 | 0.833 |
LIG_EH1_1 | 305 | 313 | PF00400 | 0.575 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.696 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.627 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.574 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.542 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.749 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.611 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.463 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.689 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.586 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.607 |
LIG_LIR_Apic_2 | 30 | 35 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 411 | 419 | PF02991 | 0.681 |
LIG_LIR_Gen_1 | 77 | 85 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 570 | 576 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.613 |
LIG_Pex14_2 | 496 | 500 | PF04695 | 0.559 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.640 |
LIG_SH2_NCK_1 | 43 | 47 | PF00017 | 0.580 |
LIG_SH2_STAP1 | 43 | 47 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 563 | 566 | PF00017 | 0.632 |
LIG_SH3_1 | 530 | 536 | PF00018 | 0.611 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.833 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.622 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.638 |
LIG_SH3_3 | 530 | 536 | PF00018 | 0.747 |
LIG_SUMO_SIM_anti_2 | 272 | 277 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 176 | 182 | PF11976 | 0.660 |
LIG_SUMO_SIM_par_1 | 446 | 452 | PF11976 | 0.693 |
LIG_WRC_WIRS_1 | 29 | 34 | PF05994 | 0.521 |
MOD_CDK_SPxxK_3 | 193 | 200 | PF00069 | 0.613 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.718 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.629 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.823 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.622 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.728 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.752 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.605 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.772 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.615 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.658 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.730 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.789 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.652 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.500 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.797 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.702 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.811 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.672 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.523 |
MOD_Cter_Amidation | 423 | 426 | PF01082 | 0.733 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.779 |
MOD_GlcNHglycan | 186 | 190 | PF01048 | 0.745 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.725 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.652 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.619 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.740 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.688 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.609 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.528 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.691 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.695 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.732 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.654 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.759 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.657 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.656 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.764 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.593 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.667 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.635 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.810 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.669 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.718 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.730 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.477 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.506 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.712 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.772 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.690 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.463 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.498 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.794 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.459 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.340 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.484 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.707 |
MOD_PIKK_1 | 440 | 446 | PF00454 | 0.735 |
MOD_PIKK_1 | 568 | 574 | PF00454 | 0.525 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.620 |
MOD_PKA_1 | 545 | 551 | PF00069 | 0.740 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.766 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.796 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.710 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.528 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.527 |
MOD_PKA_2 | 528 | 534 | PF00069 | 0.827 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.716 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.525 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.713 |
MOD_Plk_2-3 | 97 | 103 | PF00069 | 0.609 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.422 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.508 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.692 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.741 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.741 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.455 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.734 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.556 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.668 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.612 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.768 |
MOD_SUMO_rev_2 | 214 | 221 | PF00179 | 0.727 |
TRG_DiLeu_BaLyEn_6 | 300 | 305 | PF01217 | 0.523 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.296 |
TRG_ER_diArg_1 | 314 | 316 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 545 | 547 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.646 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZL6 | Leptomonas seymouri | 33% | 100% |
A0A3Q8IFE8 | Leishmania donovani | 99% | 100% |
A4HC97 | Leishmania braziliensis | 64% | 100% |
E9AVN4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 97% |
Q4QBU5 | Leishmania major | 85% | 100% |