Metal Binding, Uncharacterized
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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I9S8
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.486 |
CLV_C14_Caspase3-7 | 457 | 461 | PF00656 | 0.515 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.540 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 416 | 418 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 592 | 596 | PF00082 | 0.690 |
DEG_APCC_DBOX_1 | 103 | 111 | PF00400 | 0.446 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.546 |
DEG_SCF_FBW7_1 | 1 | 7 | PF00400 | 0.594 |
DEG_SPOP_SBC_1 | 461 | 465 | PF00917 | 0.529 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.586 |
DOC_PP2B_LxvP_1 | 278 | 281 | PF13499 | 0.530 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.577 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.630 |
LIG_14-3-3_CanoR_1 | 141 | 145 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 161 | 169 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 177 | 187 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 214 | 223 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 343 | 347 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 354 | 358 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 592 | 597 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 66 | 76 | PF00244 | 0.396 |
LIG_Actin_WH2_2 | 121 | 138 | PF00022 | 0.451 |
LIG_Actin_WH2_2 | 166 | 181 | PF00022 | 0.383 |
LIG_Actin_WH2_2 | 240 | 257 | PF00022 | 0.448 |
LIG_CaM_IQ_9 | 184 | 199 | PF13499 | 0.434 |
LIG_Clathr_ClatBox_1 | 45 | 49 | PF01394 | 0.450 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.366 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.485 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.583 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.552 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.474 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.488 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.597 |
LIG_FHA_1 | 569 | 575 | PF00498 | 0.718 |
LIG_FHA_1 | 659 | 665 | PF00498 | 0.394 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.438 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.430 |
LIG_LIR_Apic_2 | 552 | 557 | PF02991 | 0.653 |
LIG_LIR_Apic_2 | 603 | 608 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 513 | 521 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 84 | 93 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 513 | 518 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 84 | 89 | PF02991 | 0.376 |
LIG_NRBOX | 92 | 98 | PF00104 | 0.454 |
LIG_PCNA_yPIPBox_3 | 354 | 365 | PF02747 | 0.446 |
LIG_PCNA_yPIPBox_3 | 85 | 97 | PF02747 | 0.382 |
LIG_SH2_CRK | 487 | 491 | PF00017 | 0.560 |
LIG_SH2_CRK | 515 | 519 | PF00017 | 0.556 |
LIG_SH2_CRK | 545 | 549 | PF00017 | 0.526 |
LIG_SH2_CRK | 554 | 558 | PF00017 | 0.499 |
LIG_SH2_CRK | 605 | 609 | PF00017 | 0.649 |
LIG_SH2_GRB2like | 24 | 27 | PF00017 | 0.462 |
LIG_SH2_NCK_1 | 601 | 605 | PF00017 | 0.500 |
LIG_SH2_SRC | 601 | 604 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 24 | 28 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.558 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.660 |
LIG_SH3_3 | 560 | 566 | PF00018 | 0.535 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.451 |
LIG_SH3_3 | 618 | 624 | PF00018 | 0.649 |
LIG_SH3_3 | 636 | 642 | PF00018 | 0.404 |
LIG_SH3_4 | 615 | 622 | PF00018 | 0.566 |
LIG_SUMO_SIM_anti_2 | 314 | 320 | PF11976 | 0.494 |
LIG_SUMO_SIM_anti_2 | 395 | 401 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 395 | 401 | PF11976 | 0.381 |
LIG_TRAF2_1 | 145 | 148 | PF00917 | 0.394 |
LIG_TRAF2_1 | 180 | 183 | PF00917 | 0.378 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.424 |
LIG_UBA3_1 | 237 | 243 | PF00899 | 0.320 |
LIG_UBA3_1 | 396 | 400 | PF00899 | 0.477 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.514 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.493 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.484 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.594 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.643 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.546 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.450 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.397 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.547 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.463 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.538 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.432 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.576 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.455 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.496 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.548 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.472 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.669 |
MOD_GlcNHglycan | 455 | 459 | PF01048 | 0.709 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.703 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.672 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.470 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.535 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.607 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.558 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.579 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.699 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.570 |
MOD_N-GLC_1 | 392 | 397 | PF02516 | 0.468 |
MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.515 |
MOD_N-GLC_1 | 445 | 450 | PF02516 | 0.565 |
MOD_N-GLC_1 | 511 | 516 | PF02516 | 0.665 |
MOD_N-GLC_1 | 54 | 59 | PF02516 | 0.367 |
MOD_N-GLC_1 | 89 | 94 | PF02516 | 0.382 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.596 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.482 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.635 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.623 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.419 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.386 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.459 |
MOD_PIKK_1 | 178 | 184 | PF00454 | 0.270 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.407 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.453 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.529 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.463 |
MOD_PIKK_1 | 536 | 542 | PF00454 | 0.544 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.447 |
MOD_PKA_1 | 150 | 156 | PF00069 | 0.367 |
MOD_PKA_1 | 214 | 220 | PF00069 | 0.287 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.381 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.425 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.486 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.480 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.421 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.607 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.691 |
MOD_PKA_2 | 634 | 640 | PF00069 | 0.430 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.479 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.464 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.453 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.400 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.490 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.516 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.557 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.368 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.455 |
MOD_Plk_2-3 | 32 | 38 | PF00069 | 0.442 |
MOD_Plk_2-3 | 401 | 407 | PF00069 | 0.434 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.431 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.433 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.498 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.559 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.463 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.495 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.731 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.481 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.574 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.631 |
MOD_SUMO_for_1 | 169 | 172 | PF00179 | 0.353 |
MOD_SUMO_for_1 | 242 | 245 | PF00179 | 0.442 |
MOD_SUMO_for_1 | 247 | 250 | PF00179 | 0.469 |
MOD_SUMO_for_1 | 29 | 32 | PF00179 | 0.436 |
MOD_SUMO_for_1 | 418 | 421 | PF00179 | 0.455 |
MOD_SUMO_for_1 | 497 | 500 | PF00179 | 0.519 |
MOD_SUMO_for_1 | 58 | 61 | PF00179 | 0.411 |
MOD_SUMO_rev_2 | 106 | 113 | PF00179 | 0.446 |
MOD_SUMO_rev_2 | 143 | 152 | PF00179 | 0.527 |
MOD_SUMO_rev_2 | 277 | 285 | PF00179 | 0.492 |
MOD_SUMO_rev_2 | 403 | 411 | PF00179 | 0.395 |
TRG_DiLeu_BaEn_1 | 392 | 397 | PF01217 | 0.468 |
TRG_DiLeu_BaEn_1 | 41 | 46 | PF01217 | 0.459 |
TRG_DiLeu_BaEn_1 | 421 | 426 | PF01217 | 0.412 |
TRG_DiLeu_BaLyEn_6 | 374 | 379 | PF01217 | 0.355 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 515 | 518 | PF00928 | 0.556 |
TRG_ER_diArg_1 | 300 | 303 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 359 | 361 | PF00400 | 0.567 |
TRG_NES_CRM1_1 | 235 | 250 | PF08389 | 0.372 |
TRG_NES_CRM1_1 | 56 | 71 | PF08389 | 0.444 |
TRG_NLS_MonoExtC_3 | 415 | 421 | PF00514 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 300 | 304 | PF00026 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 377 | 381 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 409 | 413 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 427 | 431 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5H0 | Leptomonas seymouri | 46% | 100% |
A0A3R7KMJ4 | Trypanosoma rangeli | 26% | 100% |
A0A3S7X7R3 | Leishmania donovani | 100% | 100% |
A4HAN5 | Leishmania braziliensis | 59% | 100% |
E9B4T9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q387 | Leishmania major | 87% | 100% |
V5B3B6 | Trypanosoma cruzi | 28% | 100% |